Canonical Allele Identifier: CA369542964

Gene: BRAF

Linked Data

• MyVariant Identifiers: chr7:g.140453123C>A (hg19) ; chr7:g.140753323C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140753323C>A , CM000669.2:g.140753323C>A	GRCh38
NC_000007.13:g.140453123C>A , CM000669.1:g.140453123C>A	GRCh37
NC_000007.12:g.140099592C>A	NCBI36
NG_007873.3:g.176442G>T , LRG_299:g.176442G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.1812G>T MANE Select	ENSP00000493543.1:p.Trp604Cys
ENST00000288602.11:c.1932G>T	ENSP00000288602.7:p.Trp644Cys
ENST00000479537.6:c.482G>T
ENST00000496384.7:c.1812G>T	ENSP00000419060.2:p.Trp604Cys
ENST00000497784.2:c.*1262G>T	ENSP00000420119.2:n.*1262G>T
ENST00000642228.1:c.*890G>T	ENSP00000493678.1:n.*890G>T
ENST00000642875.1:n.1259-3905G>T
ENST00000644120.1:n.2202G>T
ENST00000644650.1:c.908G>T
ENST00000644905.1:n.2694G>T
ENST00000644969.2:c.1932G>T MANE Plus Clinical	ENSP00000496776.1:p.Trp644Cys
ENST00000646730.1:c.*388G>T	ENSP00000494784.1:n.*388G>T
ENST00000646891.1:c.1812G>T	ENSP00000493543.1:p.Trp604Cys
ENST00000647434.1:c.738-3905G>T	ENSP00000495132.1:n.738-3905G>T
ENST00000288602.10:c.1812G>T	ENSP00000288602.6:p.Trp604Cys
ENST00000479537.5:c.96G>T	ENSP00000418033.1:p.Trp32Cys
ENST00000496384.6:c.635G>T
ENST00000497784.1:c.1847G>T	ENSP00000420119.1:n.1847G>T
NM_004333.4:c.1812G>T , LRG_299t1:c.1812G>T	NP_004324.2:p.Trp604Cys
XM_005250045.1:c.1812G>T	XP_005250102.1:p.Trp604Cys
XM_005250046.1:c.1812G>T	XP_005250103.1:p.Trp604Cys
XM_011516529.1:c.1812G>T	XP_011514831.1:p.Trp604Cys
XM_011516530.1:c.1695-3905G>T	XP_011514832.1:n.1695-3905G>T
XR_242190.1:n.1820G>T
XR_927520.1:n.1820G>T
XR_927521.1:n.1820G>T
XR_927522.1:n.1703-3905G>T
XR_927523.1:n.1703-3905G>T
NM_001354609.1:c.1812G>T	NP_001341538.1:p.Trp604Cys
NM_004333.5:c.1812G>T	NP_004324.2:p.Trp604Cys
NR_148928.1:n.2910G>T
XM_017012558.1:c.1932G>T	XP_016868047.1:p.Trp644Cys
XM_017012559.1:c.1932G>T	XP_016868048.1:p.Trp644Cys
XR_001744857.1:n.1940G>T
XR_001744858.1:n.1823-3905G>T
NM_001354609.2:c.1812G>T	NP_001341538.1:p.Trp604Cys
NM_001374244.1:c.1932G>T	NP_001361173.1:p.Trp644Cys
NM_001374258.1:c.1932G>T MANE Plus Clinical	NP_001361187.1:p.Trp644Cys
NM_004333.6:c.1812G>T MANE Select	NP_004324.2:p.Trp604Cys
NM_001378467.1:c.1821G>T	NP_001365396.1:p.Trp607Cys
NM_001378468.1:c.1812G>T	NP_001365397.1:p.Trp604Cys
NM_001378469.1:c.1746G>T	NP_001365398.1:p.Trp582Cys
NM_001378470.1:c.1710G>T	NP_001365399.1:p.Trp570Cys
NM_001378471.1:c.1701G>T	NP_001365400.1:p.Trp567Cys
NM_001378472.1:c.1656G>T	NP_001365401.1:p.Trp552Cys
NM_001378473.1:c.1656G>T	NP_001365402.1:p.Trp552Cys
NM_001378474.1:c.1812G>T	NP_001365403.1:p.Trp604Cys
NM_001378475.1:c.1548G>T	NP_001365404.1:p.Trp516Cys