Canonical Allele Identifier: CA2685223926

Gene: BRAF

Linked Data

• gnomAD v4: 7-140753123-AATCT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140753126_140753129del , CM000669.2:g.140753126_140753129del	GRCh38
NC_000007.13:g.140452926_140452929del , CM000669.1:g.140452926_140452929del	GRCh37
NC_000007.12:g.140099395_140099398del	NCBI36
NG_007873.3:g.176638_176641del , LRG_299:g.176638_176641del

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.1860+148_1860+151del MANE Select	ENSP00000493543.1:n.1860+148_1860+151del
ENST00000288602.11:c.1980+148_1980+151del	ENSP00000288602.7:n.1980+148_1980+151del
ENST00000479537.6:c.530+148_530+151del
ENST00000496384.7:c.1860+148_1860+151del	ENSP00000419060.2:n.1860+148_1860+151del
ENST00000497784.2:c.*1310+148_*1310+151del	ENSP00000420119.2:n.*1310+148_*1310+151de...
ENST00000642228.1:c.*938+148_*938+151del	ENSP00000493678.1:n.*938+148_*938+151del
ENST00000642875.1:n.1259-3709_1259-3706del
ENST00000644120.1:n.2250+148_2250+151del
ENST00000644650.1:c.956+148_956+151del
ENST00000644905.1:n.2742+148_2742+151del
ENST00000644969.2:c.1980+148_1980+151del MANE Plus Clinical	ENSP00000496776.1:n.1980+148_1980+151del
ENST00000646730.1:c.*436+148_*436+151del	ENSP00000494784.1:n.*436+148_*436+151del
ENST00000646891.1:c.1860+148_1860+151del	ENSP00000493543.1:n.1860+148_1860+151del
ENST00000647434.1:c.738-3709_738-3706del	ENSP00000495132.1:n.738-3709_738-3706del
ENST00000288602.10:c.1860+148_1860+151del	ENSP00000288602.6:n.1860+148_1860+151del
ENST00000479537.5:c.144+148_144+151del	ENSP00000418033.1:n.144+148_144+151del
ENST00000496384.6:c.683+148_683+151del
ENST00000497784.1:c.1895+148_1895+151del	ENSP00000420119.1:n.1895+148_1895+151del
NM_004333.4:c.1860+148_1860+151del , LRG_299t1:c.1860+148_1860+151del	NP_004324.2:n.1860+148_1860+151del
XM_005250045.1:c.1860+148_1860+151del	XP_005250102.1:n.1860+148_1860+151del
XM_005250046.1:c.1860+148_1860+151del	XP_005250103.1:n.1860+148_1860+151del
XM_011516529.1:c.1860+148_1860+151del	XP_011514831.1:n.1860+148_1860+151del
XM_011516530.1:c.1695-3709_1695-3706del	XP_011514832.1:n.1695-3709_1695-3706del
XR_242190.1:n.1868+148_1868+151del
XR_927520.1:n.1868+148_1868+151del
XR_927521.1:n.1868+148_1868+151del
XR_927522.1:n.1703-3709_1703-3706del
XR_927523.1:n.1703-3709_1703-3706del
NM_001354609.1:c.1860+148_1860+151del	NP_001341538.1:n.1860+148_1860+151del
NM_004333.5:c.1860+148_1860+151del	NP_004324.2:n.1860+148_1860+151del
NR_148928.1:n.2958+148_2958+151del
XM_017012558.1:c.1980+148_1980+151del	XP_016868047.1:n.1980+148_1980+151del
XM_017012559.1:c.1980+148_1980+151del	XP_016868048.1:n.1980+148_1980+151del
XR_001744857.1:n.1988+148_1988+151del
XR_001744858.1:n.1823-3709_1823-3706del
NM_001354609.2:c.1860+148_1860+151del	NP_001341538.1:n.1860+148_1860+151del
NM_001374244.1:c.1980+148_1980+151del	NP_001361173.1:n.1980+148_1980+151del
NM_001374258.1:c.1980+148_1980+151del MANE Plus Clinical	NP_001361187.1:n.1980+148_1980+151del
NM_004333.6:c.1860+148_1860+151del MANE Select	NP_004324.2:n.1860+148_1860+151del
NM_001378467.1:c.1869+148_1869+151del	NP_001365396.1:n.1869+148_1869+151del
NM_001378468.1:c.1860+148_1860+151del	NP_001365397.1:n.1860+148_1860+151del
NM_001378469.1:c.1794+148_1794+151del	NP_001365398.1:n.1794+148_1794+151del
NM_001378470.1:c.1758+148_1758+151del	NP_001365399.1:n.1758+148_1758+151del
NM_001378471.1:c.1749+148_1749+151del	NP_001365400.1:n.1749+148_1749+151del
NM_001378472.1:c.1704+148_1704+151del	NP_001365401.1:n.1704+148_1704+151del
NM_001378473.1:c.1704+148_1704+151del	NP_001365402.1:n.1704+148_1704+151del
NM_001378474.1:c.1860+148_1860+151del	NP_001365403.1:n.1860+148_1860+151del
NM_001378475.1:c.1596+148_1596+151del	NP_001365404.1:n.1596+148_1596+151del