Canonical Allele Identifier: CA457987607

Gene: BRAF

Linked Data

• MyVariant Identifiers: chr7:g.140454029A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140754229A>G , CM000669.2:g.140754229A>G	GRCh38
NC_000007.13:g.140454029A>G , CM000669.1:g.140454029A>G	GRCh37
NC_000007.12:g.140100498A>G	NCBI36
NG_007873.3:g.175536T>C , LRG_299:g.175536T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1699T>C MANE Select	ENSP00000493543.1:p.Leu567=
ENST00000288602.11:c.1819T>C	ENSP00000288602.7:p.Leu607=
ENST00000479537.6:c.369T>C
ENST00000496384.7:c.1699T>C	ENSP00000419060.2:p.Leu567=
ENST00000497784.2:c.*1149T>C	ENSP00000420119.2:n.*1149T>C
ENST00000642228.1:c.*777T>C	ENSP00000493678.1:n.*777T>C
ENST00000642875.1:n.1259-4811T>C
ENST00000644120.1:n.2089T>C
ENST00000644650.1:c.795T>C
ENST00000644905.1:n.1788T>C
ENST00000644969.2:c.1819T>C MANE Plus Clinical	ENSP00000496776.1:p.Leu607=
ENST00000646730.1:c.*275T>C	ENSP00000494784.1:n.*275T>C
ENST00000646891.1:c.1699T>C	ENSP00000493543.1:p.Leu567=
ENST00000647434.1:c.738-4811T>C	ENSP00000495132.1:n.738-4811T>C
ENST00000288602.10:c.1699T>C	ENSP00000288602.6:p.Leu567=
ENST00000496384.6:c.522T>C
ENST00000497784.1:c.1734T>C	ENSP00000420119.1:n.1734T>C
NM_004333.4:c.1699T>C , LRG_299t1:c.1699T>C	NP_004324.2:p.Leu567=
XM_005250045.1:c.1699T>C	XP_005250102.1:p.Leu567=
XM_005250046.1:c.1699T>C	XP_005250103.1:p.Leu567=
XM_011516529.1:c.1699T>C	XP_011514831.1:p.Leu567=
XM_011516530.1:c.1695-4811T>C	XP_011514832.1:n.1695-4811T>C
XR_242190.1:n.1707T>C
XR_927520.1:n.1707T>C
XR_927521.1:n.1707T>C
XR_927522.1:n.1703-4811T>C
XR_927523.1:n.1703-4811T>C
NM_001354609.1:c.1699T>C	NP_001341538.1:p.Leu567=
NM_004333.5:c.1699T>C	NP_004324.2:p.Leu567=
NR_148928.1:n.2004T>C
XM_017012558.1:c.1819T>C	XP_016868047.1:p.Leu607=
XM_017012559.1:c.1819T>C	XP_016868048.1:p.Leu607=
XR_001744857.1:n.1827T>C
XR_001744858.1:n.1823-4811T>C
NM_001354609.2:c.1699T>C	NP_001341538.1:p.Leu567=
NM_001374244.1:c.1819T>C	NP_001361173.1:p.Leu607=
NM_001374258.1:c.1819T>C MANE Plus Clinical	NP_001361187.1:p.Leu607=
NM_004333.6:c.1699T>C MANE Select	NP_004324.2:p.Leu567=
NM_001378467.1:c.1708T>C	NP_001365396.1:p.Leu570=
NM_001378468.1:c.1699T>C	NP_001365397.1:p.Leu567=
NM_001378469.1:c.1633T>C	NP_001365398.1:p.Leu545=
NM_001378470.1:c.1597T>C	NP_001365399.1:p.Leu533=
NM_001378471.1:c.1588T>C	NP_001365400.1:p.Leu530=
NM_001378472.1:c.1543T>C	NP_001365401.1:p.Leu515=
NM_001378473.1:c.1543T>C	NP_001365402.1:p.Leu515=
NM_001378474.1:c.1699T>C	NP_001365403.1:p.Leu567=
NM_001378475.1:c.1435T>C	NP_001365404.1:p.Leu479=