Canonical Allele Identifier: CA1747717943

Gene: BRAF

Linked Data

• dbSNP Id: rs1800846085

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140781277A>G , CM000669.2:g.140781277A>G	GRCh38
NC_000007.13:g.140481077A>G , CM000669.1:g.140481077A>G	GRCh37
NC_000007.12:g.140127546A>G	NCBI36
NG_007873.3:g.148488T>C , LRG_299:g.148488T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1432+299T>C MANE Select	ENSP00000493543.1:n.1432+299T>C
ENST00000288602.11:c.1552+299T>C	ENSP00000288602.7:n.1552+299T>C
ENST00000479537.6:c.102+299T>C
ENST00000496384.7:c.1432+299T>C	ENSP00000419060.2:n.1432+299T>C
ENST00000497784.2:c.*882+299T>C	ENSP00000420119.2:n.*882+299T>C
ENST00000642228.1:c.*510+299T>C	ENSP00000493678.1:n.*510+299T>C
ENST00000642875.1:n.874+299T>C
ENST00000644120.1:n.1822+299T>C
ENST00000644650.1:c.528+299T>C
ENST00000644905.1:n.1521+299T>C
ENST00000644969.2:c.1552+299T>C MANE Plus Clinical	ENSP00000496776.1:n.1552+299T>C
ENST00000646334.1:n.861T>C
ENST00000646730.1:c.1432+299T>C	ENSP00000494784.1:n.1432+299T>C
ENST00000646891.1:c.1432+299T>C	ENSP00000493543.1:n.1432+299T>C
ENST00000647434.1:c.475+299T>C	ENSP00000495132.1:n.475+299T>C
ENST00000288602.10:c.1432+299T>C	ENSP00000288602.6:n.1432+299T>C
ENST00000496384.6:c.255+299T>C
ENST00000497784.1:c.1467+299T>C	ENSP00000420119.1:n.1467+299T>C
NM_004333.4:c.1432+299T>C , LRG_299t1:c.1432+299T>C	NP_004324.2:n.1432+299T>C
XM_005250045.1:c.1432+299T>C	XP_005250102.1:n.1432+299T>C
XM_005250046.1:c.1432+299T>C	XP_005250103.1:n.1432+299T>C
XM_011516529.1:c.1432+299T>C	XP_011514831.1:n.1432+299T>C
XM_011516530.1:c.1432+299T>C	XP_011514832.1:n.1432+299T>C
XR_242190.1:n.1440+299T>C
XR_927520.1:n.1440+299T>C
XR_927521.1:n.1440+299T>C
XR_927522.1:n.1440+299T>C
XR_927523.1:n.1440+299T>C
NM_001354609.1:c.1432+299T>C	NP_001341538.1:n.1432+299T>C
NM_004333.5:c.1432+299T>C	NP_004324.2:n.1432+299T>C
NR_148928.1:n.1737+299T>C
XM_017012558.1:c.1552+299T>C	XP_016868047.1:n.1552+299T>C
XM_017012559.1:c.1552+299T>C	XP_016868048.1:n.1552+299T>C
XR_001744857.1:n.1560+299T>C
XR_001744858.1:n.1560+299T>C
NM_001354609.2:c.1432+299T>C	NP_001341538.1:n.1432+299T>C
NM_001374244.1:c.1552+299T>C	NP_001361173.1:n.1552+299T>C
NM_001374258.1:c.1552+299T>C MANE Plus Clinical	NP_001361187.1:n.1552+299T>C
NM_004333.6:c.1432+299T>C MANE Select	NP_004324.2:n.1432+299T>C
NM_001378467.1:c.1441+299T>C	NP_001365396.1:n.1441+299T>C
NM_001378468.1:c.1432+299T>C	NP_001365397.1:n.1432+299T>C
NM_001378469.1:c.1366+299T>C	NP_001365398.1:n.1366+299T>C
NM_001378470.1:c.1330+299T>C	NP_001365399.1:n.1330+299T>C
NM_001378471.1:c.1321+299T>C	NP_001365400.1:n.1321+299T>C
NM_001378472.1:c.1276+299T>C	NP_001365401.1:n.1276+299T>C
NM_001378473.1:c.1276+299T>C	NP_001365402.1:n.1276+299T>C
NM_001378474.1:c.1432+299T>C	NP_001365403.1:n.1432+299T>C
NM_001378475.1:c.1168+299T>C	NP_001365404.1:n.1168+299T>C