Canonical Allele Identifier: CA2536353135

Gene: BRAF

Linked Data

• gnomAD v3: 7-140753105-T-TTC
• gnomAD v4: 7-140753105-T-TTC

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140753105_140753106insTC , CM000669.2:g.140753105_140753106insTC	GRCh38
NC_000007.13:g.140452905_140452906insTC , CM000669.1:g.140452905_140452906insTC	GRCh37
NC_000007.12:g.140099374_140099375insTC	NCBI36
NG_007873.3:g.176659_176660insGA , LRG_299:g.176659_176660insGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.1860+169_1860+170insGA MANE Select	ENSP00000493543.1:n.1860+169_1860+170insG...
ENST00000288602.11:c.1980+169_1980+170insGA	ENSP00000288602.7:n.1980+169_1980+170insG...
ENST00000479537.6:c.530+169_530+170insGA
ENST00000496384.7:c.1860+169_1860+170insGA	ENSP00000419060.2:n.1860+169_1860+170insG...
ENST00000497784.2:c.*1310+169_*1310+170insGA	ENSP00000420119.2:n.*1310+169_*1310+170in...
ENST00000642228.1:c.*938+169_*938+170insGA	ENSP00000493678.1:n.*938+169_*938+170insG...
ENST00000642875.1:n.1259-3688_1259-3687insGA
ENST00000644120.1:n.2250+169_2250+170insGA
ENST00000644650.1:c.956+169_956+170insGA
ENST00000644905.1:n.2742+169_2742+170insGA
ENST00000644969.2:c.1980+169_1980+170insGA MANE Plus Clinical	ENSP00000496776.1:n.1980+169_1980+170insG...
ENST00000646730.1:c.*436+169_*436+170insGA	ENSP00000494784.1:n.*436+169_*436+170insG...
ENST00000646891.1:c.1860+169_1860+170insGA	ENSP00000493543.1:n.1860+169_1860+170insG...
ENST00000647434.1:c.738-3688_738-3687insGA	ENSP00000495132.1:n.738-3688_738-3687insG...
ENST00000288602.10:c.1860+169_1860+170insGA	ENSP00000288602.6:n.1860+169_1860+170insG...
ENST00000479537.5:c.144+169_144+170insGA	ENSP00000418033.1:n.144+169_144+170insGA
ENST00000496384.6:c.683+169_683+170insGA
ENST00000497784.1:c.1895+169_1895+170insGA	ENSP00000420119.1:n.1895+169_1895+170insG...
NM_004333.4:c.1860+169_1860+170insGA , LRG_299t1:c.1860+169_1860+170insGA	NP_004324.2:n.1860+169_1860+170insGA
XM_005250045.1:c.1860+169_1860+170insGA	XP_005250102.1:n.1860+169_1860+170insGA
XM_005250046.1:c.1860+169_1860+170insGA	XP_005250103.1:n.1860+169_1860+170insGA
XM_011516529.1:c.1860+169_1860+170insGA	XP_011514831.1:n.1860+169_1860+170insGA
XM_011516530.1:c.1695-3688_1695-3687insGA	XP_011514832.1:n.1695-3688_1695-3687insGA...
XR_242190.1:n.1868+169_1868+170insGA
XR_927520.1:n.1868+169_1868+170insGA
XR_927521.1:n.1868+169_1868+170insGA
XR_927522.1:n.1703-3688_1703-3687insGA
XR_927523.1:n.1703-3688_1703-3687insGA
NM_001354609.1:c.1860+169_1860+170insGA	NP_001341538.1:n.1860+169_1860+170insGA
NM_004333.5:c.1860+169_1860+170insGA	NP_004324.2:n.1860+169_1860+170insGA
NR_148928.1:n.2958+169_2958+170insGA
XM_017012558.1:c.1980+169_1980+170insGA	XP_016868047.1:n.1980+169_1980+170insGA
XM_017012559.1:c.1980+169_1980+170insGA	XP_016868048.1:n.1980+169_1980+170insGA
XR_001744857.1:n.1988+169_1988+170insGA
XR_001744858.1:n.1823-3688_1823-3687insGA
NM_001354609.2:c.1860+169_1860+170insGA	NP_001341538.1:n.1860+169_1860+170insGA
NM_001374244.1:c.1980+169_1980+170insGA	NP_001361173.1:n.1980+169_1980+170insGA
NM_001374258.1:c.1980+169_1980+170insGA MANE Plus Clinical	NP_001361187.1:n.1980+169_1980+170insGA
NM_004333.6:c.1860+169_1860+170insGA MANE Select	NP_004324.2:n.1860+169_1860+170insGA
NM_001378467.1:c.1869+169_1869+170insGA	NP_001365396.1:n.1869+169_1869+170insGA
NM_001378468.1:c.1860+169_1860+170insGA	NP_001365397.1:n.1860+169_1860+170insGA
NM_001378469.1:c.1794+169_1794+170insGA	NP_001365398.1:n.1794+169_1794+170insGA
NM_001378470.1:c.1758+169_1758+170insGA	NP_001365399.1:n.1758+169_1758+170insGA
NM_001378471.1:c.1749+169_1749+170insGA	NP_001365400.1:n.1749+169_1749+170insGA
NM_001378472.1:c.1704+169_1704+170insGA	NP_001365401.1:n.1704+169_1704+170insGA
NM_001378473.1:c.1704+169_1704+170insGA	NP_001365402.1:n.1704+169_1704+170insGA
NM_001378474.1:c.1860+169_1860+170insGA	NP_001365403.1:n.1860+169_1860+170insGA
NM_001378475.1:c.1596+169_1596+170insGA	NP_001365404.1:n.1596+169_1596+170insGA