Canonical Allele Identifier: CA1107945532

Gene: BRAF

Linked Data

• dbSNP Id: rs1797908532

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140753007_140753009del , CM000669.2:g.140753007_140753009del	GRCh38
NC_000007.13:g.140452807_140452809del , CM000669.1:g.140452807_140452809del	GRCh37
NC_000007.12:g.140099276_140099278del	NCBI36
NG_007873.3:g.176757_176759del , LRG_299:g.176757_176759del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1860+267_1860+269del MANE Select	ENSP00000493543.1:n.1860+267_1860+269del
ENST00000288602.11:c.1980+267_1980+269del	ENSP00000288602.7:n.1980+267_1980+269del
ENST00000479537.6:c.530+267_530+269del
ENST00000496384.7:c.1860+267_1860+269del	ENSP00000419060.2:n.1860+267_1860+269del
ENST00000497784.2:c.*1310+267_*1310+269del	ENSP00000420119.2:n.*1310+267_*1310+269del
ENST00000642228.1:c.*938+267_*938+269del	ENSP00000493678.1:n.*938+267_*938+269del
ENST00000642875.1:n.1259-3590_1259-3588del
ENST00000644120.1:n.2250+267_2250+269del
ENST00000644650.1:c.956+267_956+269del
ENST00000644905.1:n.2742+267_2742+269del
ENST00000644969.2:c.1980+267_1980+269del MANE Plus Clinical	ENSP00000496776.1:n.1980+267_1980+269del
ENST00000646730.1:c.*436+267_*436+269del	ENSP00000494784.1:n.*436+267_*436+269del
ENST00000646891.1:c.1860+267_1860+269del	ENSP00000493543.1:n.1860+267_1860+269del
ENST00000647434.1:c.738-3590_738-3588del	ENSP00000495132.1:n.738-3590_738-3588del
ENST00000288602.10:c.1860+267_1860+269del	ENSP00000288602.6:n.1860+267_1860+269del
ENST00000479537.5:c.144+267_144+269del	ENSP00000418033.1:n.144+267_144+269del
ENST00000496384.6:c.683+267_683+269del
ENST00000497784.1:c.1895+267_1895+269del	ENSP00000420119.1:n.1895+267_1895+269del
NM_004333.4:c.1860+267_1860+269del , LRG_299t1:c.1860+267_1860+269del	NP_004324.2:n.1860+267_1860+269del
XM_005250045.1:c.1860+267_1860+269del	XP_005250102.1:n.1860+267_1860+269del
XM_005250046.1:c.1860+267_1860+269del	XP_005250103.1:n.1860+267_1860+269del
XM_011516529.1:c.1860+267_1860+269del	XP_011514831.1:n.1860+267_1860+269del
XM_011516530.1:c.1695-3590_1695-3588del	XP_011514832.1:n.1695-3590_1695-3588del
XR_242190.1:n.1868+267_1868+269del
XR_927520.1:n.1868+267_1868+269del
XR_927521.1:n.1868+267_1868+269del
XR_927522.1:n.1703-3590_1703-3588del
XR_927523.1:n.1703-3590_1703-3588del
NM_001354609.1:c.1860+267_1860+269del	NP_001341538.1:n.1860+267_1860+269del
NM_004333.5:c.1860+267_1860+269del	NP_004324.2:n.1860+267_1860+269del
NR_148928.1:n.2958+267_2958+269del
XM_017012558.1:c.1980+267_1980+269del	XP_016868047.1:n.1980+267_1980+269del
XM_017012559.1:c.1980+267_1980+269del	XP_016868048.1:n.1980+267_1980+269del
XR_001744857.1:n.1988+267_1988+269del
XR_001744858.1:n.1823-3590_1823-3588del
NM_001354609.2:c.1860+267_1860+269del	NP_001341538.1:n.1860+267_1860+269del
NM_001374244.1:c.1980+267_1980+269del	NP_001361173.1:n.1980+267_1980+269del
NM_001374258.1:c.1980+267_1980+269del MANE Plus Clinical	NP_001361187.1:n.1980+267_1980+269del
NM_004333.6:c.1860+267_1860+269del MANE Select	NP_004324.2:n.1860+267_1860+269del
NM_001378467.1:c.1869+267_1869+269del	NP_001365396.1:n.1869+267_1869+269del
NM_001378468.1:c.1860+267_1860+269del	NP_001365397.1:n.1860+267_1860+269del
NM_001378469.1:c.1794+267_1794+269del	NP_001365398.1:n.1794+267_1794+269del
NM_001378470.1:c.1758+267_1758+269del	NP_001365399.1:n.1758+267_1758+269del
NM_001378471.1:c.1749+267_1749+269del	NP_001365400.1:n.1749+267_1749+269del
NM_001378472.1:c.1704+267_1704+269del	NP_001365401.1:n.1704+267_1704+269del
NM_001378473.1:c.1704+267_1704+269del	NP_001365402.1:n.1704+267_1704+269del
NM_001378474.1:c.1860+267_1860+269del	NP_001365403.1:n.1860+267_1860+269del
NM_001378475.1:c.1596+267_1596+269del	NP_001365404.1:n.1596+267_1596+269del