Canonical Allele Identifier: CA2685223934

Gene: BRAF

Linked Data

• gnomAD v4: 7-140753135-T-TAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140753141_140753142insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA , CM000669.2:g.140753141_140753142insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	GRCh38
NC_000007.13:g.140452941_140452942insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA , CM000669.1:g.140452941_140452942insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	GRCh37
NC_000007.12:g.140099410_140099411insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NCBI36
NG_007873.3:g.176629_176630insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT , LRG_299:g.176629_176630insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.1860+139_1860+140insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select	ENSP00000493543.1:n.1860+139_1860+140insT...
ENST00000288602.11:c.1980+139_1980+140insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000288602.7:n.1980+139_1980+140insT...
ENST00000479537.6:c.530+139_530+140insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000496384.7:c.1860+139_1860+140insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000419060.2:n.1860+139_1860+140insT...
ENST00000497784.2:c.*1310+139_*1310+140insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000420119.2:n.*1310+139_*1310+140in...
ENST00000642228.1:c.*938+139_*938+140insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000493678.1:n.*938+139_*938+140insT...
ENST00000642875.1:n.1259-3718_1259-3717insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000644120.1:n.2250+139_2250+140insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000644650.1:c.956+139_956+140insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000644905.1:n.2742+139_2742+140insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000644969.2:c.1980+139_1980+140insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Plus Clinical	ENSP00000496776.1:n.1980+139_1980+140insT...
ENST00000646730.1:c.*436+139_*436+140insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000494784.1:n.*436+139_*436+140insT...
ENST00000646891.1:c.1860+139_1860+140insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000493543.1:n.1860+139_1860+140insT...
ENST00000647434.1:c.738-3718_738-3717insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000495132.1:n.738-3718_738-3717insT...
ENST00000288602.10:c.1860+139_1860+140insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000288602.6:n.1860+139_1860+140insT...
ENST00000479537.5:c.144+139_144+140insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000418033.1:n.144+139_144+140insTTT...
ENST00000496384.6:c.683+139_683+140insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000497784.1:c.1895+139_1895+140insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000420119.1:n.1895+139_1895+140insT...
NM_004333.4:c.1860+139_1860+140insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT , LRG_299t1:c.1860+139_1860+140insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NP_004324.2:n.1860+139_1860+140insTTTTTTT...
XM_005250045.1:c.1860+139_1860+140insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_005250102.1:n.1860+139_1860+140insTTTT...
XM_005250046.1:c.1860+139_1860+140insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_005250103.1:n.1860+139_1860+140insTTTT...
XM_011516529.1:c.1860+139_1860+140insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_011514831.1:n.1860+139_1860+140insTTTT...
XM_011516530.1:c.1695-3718_1695-3717insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_011514832.1:n.1695-3718_1695-3717insTT...
XR_242190.1:n.1868+139_1868+140insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
XR_927520.1:n.1868+139_1868+140insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
XR_927521.1:n.1868+139_1868+140insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
XR_927522.1:n.1703-3718_1703-3717insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
XR_927523.1:n.1703-3718_1703-3717insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
NM_001354609.1:c.1860+139_1860+140insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NP_001341538.1:n.1860+139_1860+140insTTTT...
NM_004333.5:c.1860+139_1860+140insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NP_004324.2:n.1860+139_1860+140insTTTTTTT...
NR_148928.1:n.2958+139_2958+140insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
XM_017012558.1:c.1980+139_1980+140insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_016868047.1:n.1980+139_1980+140insTTTT...
XM_017012559.1:c.1980+139_1980+140insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_016868048.1:n.1980+139_1980+140insTTTT...
XR_001744857.1:n.1988+139_1988+140insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
XR_001744858.1:n.1823-3718_1823-3717insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
NM_001354609.2:c.1860+139_1860+140insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NP_001341538.1:n.1860+139_1860+140insTTTT...
NM_001374244.1:c.1980+139_1980+140insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NP_001361173.1:n.1980+139_1980+140insTTTT...
NM_001374258.1:c.1980+139_1980+140insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Plus Clinical	NP_001361187.1:n.1980+139_1980+140insTTTT...
NM_004333.6:c.1860+139_1860+140insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select	NP_004324.2:n.1860+139_1860+140insTTTTTTT...
NM_001378467.1:c.1869+139_1869+140insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NP_001365396.1:n.1869+139_1869+140insTTTT...
NM_001378468.1:c.1860+139_1860+140insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NP_001365397.1:n.1860+139_1860+140insTTTT...
NM_001378469.1:c.1794+139_1794+140insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NP_001365398.1:n.1794+139_1794+140insTTTT...
NM_001378470.1:c.1758+139_1758+140insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NP_001365399.1:n.1758+139_1758+140insTTTT...
NM_001378471.1:c.1749+139_1749+140insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NP_001365400.1:n.1749+139_1749+140insTTTT...
NM_001378472.1:c.1704+139_1704+140insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NP_001365401.1:n.1704+139_1704+140insTTTT...
NM_001378473.1:c.1704+139_1704+140insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NP_001365402.1:n.1704+139_1704+140insTTTT...
NM_001378474.1:c.1860+139_1860+140insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NP_001365403.1:n.1860+139_1860+140insTTTT...
NM_001378475.1:c.1596+139_1596+140insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NP_001365404.1:n.1596+139_1596+140insTTTT...