Canonical Allele Identifier: CA369588169

Gene: BRAF

Linked Data

• dbSNP Id: rs397507479
• MyVariant Identifiers: chr7:g.140476811C>G (hg19) ; chr7:g.140777011C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140777011C>G , CM000669.2:g.140777011C>G	GRCh38
NC_000007.13:g.140476811C>G , CM000669.1:g.140476811C>G	GRCh37
NC_000007.12:g.140123280C>G	NCBI36
NG_007873.3:g.152754G>C , LRG_299:g.152754G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1595G>C MANE Select	ENSP00000493543.1:p.Cys532Ser
ENST00000288602.11:c.1715G>C	ENSP00000288602.7:p.Cys572Ser
ENST00000479537.6:c.265G>C
ENST00000496384.7:c.1595G>C	ENSP00000419060.2:p.Cys532Ser
ENST00000497784.2:c.*1045G>C	ENSP00000420119.2:n.*1045G>C
ENST00000642228.1:c.*673G>C	ENSP00000493678.1:n.*673G>C
ENST00000642875.1:n.1159G>C
ENST00000644120.1:n.1985G>C
ENST00000644650.1:c.691G>C
ENST00000644905.1:n.1684G>C
ENST00000644969.2:c.1715G>C MANE Plus Clinical	ENSP00000496776.1:p.Cys572Ser
ENST00000646730.1:c.1595G>C	ENSP00000494784.1:p.Cys532Ser
ENST00000646891.1:c.1595G>C	ENSP00000493543.1:p.Cys532Ser
ENST00000647434.1:c.638G>C	ENSP00000495132.1:p.Cys213Ser
ENST00000288602.10:c.1595G>C	ENSP00000288602.6:p.Cys532Ser
ENST00000496384.6:c.418G>C
ENST00000497784.1:c.1630G>C	ENSP00000420119.1:n.1630G>C
NM_004333.4:c.1595G>C , LRG_299t1:c.1595G>C	NP_004324.2:p.Cys532Ser
XM_005250045.1:c.1595G>C	XP_005250102.1:p.Cys532Ser
XM_005250046.1:c.1595G>C	XP_005250103.1:p.Cys532Ser
XM_011516529.1:c.1595G>C	XP_011514831.1:p.Cys532Ser
XM_011516530.1:c.1595G>C	XP_011514832.1:p.Cys532Ser
XR_242190.1:n.1603G>C
XR_927520.1:n.1603G>C
XR_927521.1:n.1603G>C
XR_927522.1:n.1603G>C
XR_927523.1:n.1603G>C
NM_001354609.1:c.1595G>C	NP_001341538.1:p.Cys532Ser
NM_004333.5:c.1595G>C	NP_004324.2:p.Cys532Ser
NR_148928.1:n.1900G>C
XM_017012558.1:c.1715G>C	XP_016868047.1:p.Cys572Ser
XM_017012559.1:c.1715G>C	XP_016868048.1:p.Cys572Ser
XR_001744857.1:n.1723G>C
XR_001744858.1:n.1723G>C
NM_001354609.2:c.1595G>C	NP_001341538.1:p.Cys532Ser
NM_001374244.1:c.1715G>C	NP_001361173.1:p.Cys572Ser
NM_001374258.1:c.1715G>C MANE Plus Clinical	NP_001361187.1:p.Cys572Ser
NM_004333.6:c.1595G>C MANE Select	NP_004324.2:p.Cys532Ser
NM_001378467.1:c.1604G>C	NP_001365396.1:p.Cys535Ser
NM_001378468.1:c.1595G>C	NP_001365397.1:p.Cys532Ser
NM_001378469.1:c.1529G>C	NP_001365398.1:p.Cys510Ser
NM_001378470.1:c.1493G>C	NP_001365399.1:p.Cys498Ser
NM_001378471.1:c.1484G>C	NP_001365400.1:p.Cys495Ser
NM_001378472.1:c.1439G>C	NP_001365401.1:p.Cys480Ser
NM_001378473.1:c.1439G>C	NP_001365402.1:p.Cys480Ser
NM_001378474.1:c.1595G>C	NP_001365403.1:p.Cys532Ser
NM_001378475.1:c.1331G>C	NP_001365404.1:p.Cys444Ser