Canonical Allele Identifier: CA369588913

Gene: BRAF

Linked Data

• MyVariant Identifiers: chr7:g.140481426T>G (hg19) ; chr7:g.140781626T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140781626T>G , CM000669.2:g.140781626T>G	GRCh38
NC_000007.13:g.140481426T>G , CM000669.1:g.140481426T>G	GRCh37
NC_000007.12:g.140127895T>G	NCBI36
NG_007873.3:g.148139A>C , LRG_299:g.148139A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.1382A>C MANE Select	ENSP00000493543.1:p.Gln461Pro
ENST00000288602.11:c.1502A>C	ENSP00000288602.7:p.Gln501Pro
ENST00000479537.6:c.52A>C
ENST00000496384.7:c.1382A>C	ENSP00000419060.2:p.Gln461Pro
ENST00000497784.2:c.*832A>C	ENSP00000420119.2:n.*832A>C
ENST00000642228.1:c.*460A>C	ENSP00000493678.1:n.*460A>C
ENST00000642875.1:n.824A>C
ENST00000644120.1:n.1772A>C
ENST00000644650.1:c.478A>C
ENST00000644905.1:n.1471A>C
ENST00000644969.2:c.1502A>C MANE Plus Clinical	ENSP00000496776.1:p.Gln501Pro
ENST00000646334.1:n.512A>C
ENST00000646730.1:c.1382A>C	ENSP00000494784.1:p.Gln461Pro
ENST00000646891.1:c.1382A>C	ENSP00000493543.1:p.Gln461Pro
ENST00000647434.1:c.425A>C	ENSP00000495132.1:p.Gln142Pro
ENST00000288602.10:c.1382A>C	ENSP00000288602.6:p.Gln461Pro
ENST00000496384.6:c.205A>C
ENST00000497784.1:c.1417A>C	ENSP00000420119.1:n.1417A>C
NM_004333.4:c.1382A>C , LRG_299t1:c.1382A>C	NP_004324.2:p.Gln461Pro
XM_005250045.1:c.1382A>C	XP_005250102.1:p.Gln461Pro
XM_005250046.1:c.1382A>C	XP_005250103.1:p.Gln461Pro
XM_011516529.1:c.1382A>C	XP_011514831.1:p.Gln461Pro
XM_011516530.1:c.1382A>C	XP_011514832.1:p.Gln461Pro
XR_242190.1:n.1390A>C
XR_927520.1:n.1390A>C
XR_927521.1:n.1390A>C
XR_927522.1:n.1390A>C
XR_927523.1:n.1390A>C
NM_001354609.1:c.1382A>C	NP_001341538.1:p.Gln461Pro
NM_004333.5:c.1382A>C	NP_004324.2:p.Gln461Pro
NR_148928.1:n.1687A>C
XM_017012558.1:c.1502A>C	XP_016868047.1:p.Gln501Pro
XM_017012559.1:c.1502A>C	XP_016868048.1:p.Gln501Pro
XR_001744857.1:n.1510A>C
XR_001744858.1:n.1510A>C
NM_001354609.2:c.1382A>C	NP_001341538.1:p.Gln461Pro
NM_001374244.1:c.1502A>C	NP_001361173.1:p.Gln501Pro
NM_001374258.1:c.1502A>C MANE Plus Clinical	NP_001361187.1:p.Gln501Pro
NM_004333.6:c.1382A>C MANE Select	NP_004324.2:p.Gln461Pro
NM_001378467.1:c.1391A>C	NP_001365396.1:p.Gln464Pro
NM_001378468.1:c.1382A>C	NP_001365397.1:p.Gln461Pro
NM_001378469.1:c.1316A>C	NP_001365398.1:p.Gln439Pro
NM_001378470.1:c.1280A>C	NP_001365399.1:p.Gln427Pro
NM_001378471.1:c.1271A>C	NP_001365400.1:p.Gln424Pro
NM_001378472.1:c.1226A>C	NP_001365401.1:p.Gln409Pro
NM_001378473.1:c.1226A>C	NP_001365402.1:p.Gln409Pro
NM_001378474.1:c.1382A>C	NP_001365403.1:p.Gln461Pro
NM_001378475.1:c.1118A>C	NP_001365404.1:p.Gln373Pro