Canonical Allele Identifier: CA2715924775

Gene: BRAF

Linked Data

• dbSNP Id: rs2128994241

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140749277A>T , CM000669.2:g.140749277A>T	GRCh38
NC_000007.13:g.140449077A>T , CM000669.1:g.140449077A>T	GRCh37
NC_000007.12:g.140095546A>T	NCBI36
NG_007873.3:g.180488T>A , LRG_299:g.180488T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1992+10T>A MANE Select	ENSP00000493543.1:n.1992+10T>A
ENST00000288602.11:c.2112+10T>A	ENSP00000288602.7:n.2112+10T>A
ENST00000479537.6:c.662+10T>A
ENST00000496384.7:c.1992+10T>A	ENSP00000419060.2:n.1992+10T>A
ENST00000497784.2:c.*1442+10T>A	ENSP00000420119.2:n.*1442+10T>A
ENST00000642228.1:c.*1070+10T>A	ENSP00000493678.1:n.*1070+10T>A
ENST00000642875.1:n.1390+10T>A
ENST00000644120.1:n.2382+10T>A
ENST00000644650.1:c.1088+10T>A
ENST00000644905.1:n.2874+10T>A
ENST00000644969.2:c.2112+10T>A MANE Plus Clinical	ENSP00000496776.1:n.2112+10T>A
ENST00000646730.1:c.*568+10T>A	ENSP00000494784.1:n.*568+10T>A
ENST00000646891.1:c.1992+10T>A	ENSP00000493543.1:n.1992+10T>A
ENST00000647434.1:c.869+10T>A	ENSP00000495132.1:n.869+10T>A
ENST00000288602.10:c.1992+10T>A	ENSP00000288602.6:n.1992+10T>A
ENST00000479537.5:c.276+10T>A	ENSP00000418033.1:n.276+10T>A
ENST00000496384.6:c.815+10T>A
ENST00000497784.1:c.2027+10T>A	ENSP00000420119.1:n.2027+10T>A
NM_004333.4:c.1992+10T>A , LRG_299t1:c.1992+10T>A	NP_004324.2:n.1992+10T>A
XM_005250045.1:c.1992+10T>A	XP_005250102.1:n.1992+10T>A
XM_005250046.1:c.1992+10T>A	XP_005250103.1:n.1992+10T>A
XM_011516529.1:c.1992+10T>A	XP_011514831.1:n.1992+10T>A
XM_011516530.1:c.*44+10T>A	XP_011514832.1:n.*44+10T>A
XR_242190.1:n.2000+10T>A
XR_927520.1:n.2000+10T>A
XR_927521.1:n.2000+10T>A
XR_927522.1:n.1834+10T>A
XR_927523.1:n.1834+10T>A
NM_001354609.1:c.1992+10T>A	NP_001341538.1:n.1992+10T>A
NM_004333.5:c.1992+10T>A	NP_004324.2:n.1992+10T>A
NR_148928.1:n.3090+10T>A
XM_017012558.1:c.2112+10T>A	XP_016868047.1:n.2112+10T>A
XM_017012559.1:c.2112+10T>A	XP_016868048.1:n.2112+10T>A
XR_001744857.1:n.2120+10T>A
XR_001744858.1:n.1954+10T>A
NM_001354609.2:c.1992+10T>A	NP_001341538.1:n.1992+10T>A
NM_001374244.1:c.2112+10T>A	NP_001361173.1:n.2112+10T>A
NM_001374258.1:c.2112+10T>A MANE Plus Clinical	NP_001361187.1:n.2112+10T>A
NM_004333.6:c.1992+10T>A MANE Select	NP_004324.2:n.1992+10T>A
NM_001378467.1:c.2001+10T>A	NP_001365396.1:n.2001+10T>A
NM_001378468.1:c.1992+10T>A	NP_001365397.1:n.1992+10T>A
NM_001378469.1:c.1926+10T>A	NP_001365398.1:n.1926+10T>A
NM_001378470.1:c.1890+10T>A	NP_001365399.1:n.1890+10T>A
NM_001378471.1:c.1881+10T>A	NP_001365400.1:n.1881+10T>A
NM_001378472.1:c.1836+10T>A	NP_001365401.1:n.1836+10T>A
NM_001378473.1:c.1836+10T>A	NP_001365402.1:n.1836+10T>A
NM_001378474.1:c.1992+10T>A	NP_001365403.1:n.1992+10T>A
NM_001378475.1:c.1728+10T>A	NP_001365404.1:n.1728+10T>A