Canonical Allele Identifier: CA369541112

Gene: BRAF

Linked Data

• dbSNP Id: rs2128994533
• MyVariant Identifiers: chr7:g.140449178C>G (hg19) ; chr7:g.140749378C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140749378C>G , CM000669.2:g.140749378C>G	GRCh38
NC_000007.13:g.140449178C>G , CM000669.1:g.140449178C>G	GRCh37
NC_000007.12:g.140095647C>G	NCBI36
NG_007873.3:g.180387G>C , LRG_299:g.180387G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1901G>C MANE Select	ENSP00000493543.1:p.Ser634Thr
ENST00000288602.11:c.2021G>C	ENSP00000288602.7:p.Ser674Thr
ENST00000479537.6:c.571G>C
ENST00000496384.7:c.1901G>C	ENSP00000419060.2:p.Ser634Thr
ENST00000497784.2:c.*1351G>C	ENSP00000420119.2:n.*1351G>C
ENST00000642228.1:c.*979G>C	ENSP00000493678.1:n.*979G>C
ENST00000642875.1:n.1299G>C
ENST00000644120.1:n.2291G>C
ENST00000644650.1:c.997G>C
ENST00000644905.1:n.2783G>C
ENST00000644969.2:c.2021G>C MANE Plus Clinical	ENSP00000496776.1:p.Ser674Thr
ENST00000646730.1:c.*477G>C	ENSP00000494784.1:n.*477G>C
ENST00000646891.1:c.1901G>C	ENSP00000493543.1:p.Ser634Thr
ENST00000647434.1:c.778G>C	ENSP00000495132.1:p.Ala260Pro
ENST00000288602.10:c.1901G>C	ENSP00000288602.6:p.Ser634Thr
ENST00000479537.5:c.185G>C	ENSP00000418033.1:p.Ser62Thr
ENST00000496384.6:c.724G>C
ENST00000497784.1:c.1936G>C	ENSP00000420119.1:n.1936G>C
NM_004333.4:c.1901G>C , LRG_299t1:c.1901G>C	NP_004324.2:p.Ser634Thr
XM_005250045.1:c.1901G>C	XP_005250102.1:p.Ser634Thr
XM_005250046.1:c.1901G>C	XP_005250103.1:p.Ser634Thr
XM_011516529.1:c.1901G>C	XP_011514831.1:p.Ser634Thr
XM_011516530.1:c.1735G>C	XP_011514832.1:p.Ala579Pro
XR_242190.1:n.1909G>C
XR_927520.1:n.1909G>C
XR_927521.1:n.1909G>C
XR_927522.1:n.1743G>C
XR_927523.1:n.1743G>C
NM_001354609.1:c.1901G>C	NP_001341538.1:p.Ser634Thr
NM_004333.5:c.1901G>C	NP_004324.2:p.Ser634Thr
NR_148928.1:n.2999G>C
XM_017012558.1:c.2021G>C	XP_016868047.1:p.Ser674Thr
XM_017012559.1:c.2021G>C	XP_016868048.1:p.Ser674Thr
XR_001744857.1:n.2029G>C
XR_001744858.1:n.1863G>C
NM_001354609.2:c.1901G>C	NP_001341538.1:p.Ser634Thr
NM_001374244.1:c.2021G>C	NP_001361173.1:p.Ser674Thr
NM_001374258.1:c.2021G>C MANE Plus Clinical	NP_001361187.1:p.Ser674Thr
NM_004333.6:c.1901G>C MANE Select	NP_004324.2:p.Ser634Thr
NM_001378467.1:c.1910G>C	NP_001365396.1:p.Ser637Thr
NM_001378468.1:c.1901G>C	NP_001365397.1:p.Ser634Thr
NM_001378469.1:c.1835G>C	NP_001365398.1:p.Ser612Thr
NM_001378470.1:c.1799G>C	NP_001365399.1:p.Ser600Thr
NM_001378471.1:c.1790G>C	NP_001365400.1:p.Ser597Thr
NM_001378472.1:c.1745G>C	NP_001365401.1:p.Ser582Thr
NM_001378473.1:c.1745G>C	NP_001365402.1:p.Ser582Thr
NM_001378474.1:c.1901G>C	NP_001365403.1:p.Ser634Thr
NM_001378475.1:c.1637G>C	NP_001365404.1:p.Ser546Thr