Canonical Allele Identifier: CA1747709884

Gene: BRAF

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140753036_140753038delinsACT , CM000669.2:g.140753036_140753038delinsACT	GRCh38
NC_000007.13:g.140452836_140452838delinsACT , CM000669.1:g.140452836_140452838delinsACT	GRCh37
NC_000007.12:g.140099305_140099307delinsACT	NCBI36
NG_007873.3:g.176727_176729delinsAGT , LRG_299:g.176727_176729delinsAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1860+237_1860+239delinsAGT MANE Select	ENSP00000493543.1:n.1860+237_1860+239delinsAGT
ENST00000288602.11:c.1980+237_1980+239delinsAGT	ENSP00000288602.7:n.1980+237_1980+239delinsAGT
ENST00000479537.6:c.530+237_530+239delinsAGT
ENST00000496384.7:c.1860+237_1860+239delinsAGT	ENSP00000419060.2:n.1860+237_1860+239delinsAGT
ENST00000497784.2:c.*1310+237_*1310+239delinsAGT	ENSP00000420119.2:n.*1310+237_*1310+239delinsAGT
ENST00000642228.1:c.*938+237_*938+239delinsAGT	ENSP00000493678.1:n.*938+237_*938+239delinsAGT
ENST00000642875.1:n.1259-3620_1259-3618delinsAGT
ENST00000644120.1:n.2250+237_2250+239delinsAGT
ENST00000644650.1:c.956+237_956+239delinsAGT
ENST00000644905.1:n.2742+237_2742+239delinsAGT
ENST00000644969.2:c.1980+237_1980+239delinsAGT MANE Plus Clinical	ENSP00000496776.1:n.1980+237_1980+239delinsAGT
ENST00000646730.1:c.*436+237_*436+239delinsAGT	ENSP00000494784.1:n.*436+237_*436+239delinsAGT
ENST00000646891.1:c.1860+237_1860+239delinsAGT	ENSP00000493543.1:n.1860+237_1860+239delinsAGT
ENST00000647434.1:c.738-3620_738-3618delinsAGT	ENSP00000495132.1:n.738-3620_738-3618delinsAGT
ENST00000288602.10:c.1860+237_1860+239delinsAGT	ENSP00000288602.6:n.1860+237_1860+239delinsAGT
ENST00000479537.5:c.144+237_144+239delinsAGT	ENSP00000418033.1:n.144+237_144+239delinsAGT
ENST00000496384.6:c.683+237_683+239delinsAGT
ENST00000497784.1:c.1895+237_1895+239delinsAGT	ENSP00000420119.1:n.1895+237_1895+239delinsAGT
NM_004333.4:c.1860+237_1860+239delinsAGT , LRG_299t1:c.1860+237_1860+239delinsAGT	NP_004324.2:n.1860+237_1860+239delinsAGT
XM_005250045.1:c.1860+237_1860+239delinsAGT	XP_005250102.1:n.1860+237_1860+239delinsAGT
XM_005250046.1:c.1860+237_1860+239delinsAGT	XP_005250103.1:n.1860+237_1860+239delinsAGT
XM_011516529.1:c.1860+237_1860+239delinsAGT	XP_011514831.1:n.1860+237_1860+239delinsAGT
XM_011516530.1:c.1695-3620_1695-3618delinsAGT	XP_011514832.1:n.1695-3620_1695-3618delinsAGT
XR_242190.1:n.1868+237_1868+239delinsAGT
XR_927520.1:n.1868+237_1868+239delinsAGT
XR_927521.1:n.1868+237_1868+239delinsAGT
XR_927522.1:n.1703-3620_1703-3618delinsAGT
XR_927523.1:n.1703-3620_1703-3618delinsAGT
NM_001354609.1:c.1860+237_1860+239delinsAGT	NP_001341538.1:n.1860+237_1860+239delinsAGT
NM_004333.5:c.1860+237_1860+239delinsAGT	NP_004324.2:n.1860+237_1860+239delinsAGT
NR_148928.1:n.2958+237_2958+239delinsAGT
XM_017012558.1:c.1980+237_1980+239delinsAGT	XP_016868047.1:n.1980+237_1980+239delinsAGT
XM_017012559.1:c.1980+237_1980+239delinsAGT	XP_016868048.1:n.1980+237_1980+239delinsAGT
XR_001744857.1:n.1988+237_1988+239delinsAGT
XR_001744858.1:n.1823-3620_1823-3618delinsAGT
NM_001354609.2:c.1860+237_1860+239delinsAGT	NP_001341538.1:n.1860+237_1860+239delinsAGT
NM_001374244.1:c.1980+237_1980+239delinsAGT	NP_001361173.1:n.1980+237_1980+239delinsAGT
NM_001374258.1:c.1980+237_1980+239delinsAGT MANE Plus Clinical	NP_001361187.1:n.1980+237_1980+239delinsAGT
NM_004333.6:c.1860+237_1860+239delinsAGT MANE Select	NP_004324.2:n.1860+237_1860+239delinsAGT
NM_001378467.1:c.1869+237_1869+239delinsAGT	NP_001365396.1:n.1869+237_1869+239delinsAGT
NM_001378468.1:c.1860+237_1860+239delinsAGT	NP_001365397.1:n.1860+237_1860+239delinsAGT
NM_001378469.1:c.1794+237_1794+239delinsAGT	NP_001365398.1:n.1794+237_1794+239delinsAGT
NM_001378470.1:c.1758+237_1758+239delinsAGT	NP_001365399.1:n.1758+237_1758+239delinsAGT
NM_001378471.1:c.1749+237_1749+239delinsAGT	NP_001365400.1:n.1749+237_1749+239delinsAGT
NM_001378472.1:c.1704+237_1704+239delinsAGT	NP_001365401.1:n.1704+237_1704+239delinsAGT
NM_001378473.1:c.1704+237_1704+239delinsAGT	NP_001365402.1:n.1704+237_1704+239delinsAGT
NM_001378474.1:c.1860+237_1860+239delinsAGT	NP_001365403.1:n.1860+237_1860+239delinsAGT
NM_001378475.1:c.1596+237_1596+239delinsAGT	NP_001365404.1:n.1596+237_1596+239delinsAGT