Canonical Allele Identifier: CA458115635

Gene: BRAF

Linked Data

• dbSNP Id: rs1269507461
• MyVariant Identifiers: chr7:g.140476861G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140777061G>A , CM000669.2:g.140777061G>A	GRCh38
NC_000007.13:g.140476861G>A , CM000669.1:g.140476861G>A	GRCh37
NC_000007.12:g.140123330G>A	NCBI36
NG_007873.3:g.152704C>T , LRG_299:g.152704C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1545C>T MANE Select	ENSP00000493543.1:p.Leu515=
ENST00000288602.11:c.1665C>T	ENSP00000288602.7:p.Leu555=
ENST00000479537.6:c.215C>T
ENST00000496384.7:c.1545C>T	ENSP00000419060.2:p.Leu515=
ENST00000497784.2:c.*995C>T	ENSP00000420119.2:n.*995C>T
ENST00000642228.1:c.*623C>T	ENSP00000493678.1:n.*623C>T
ENST00000642875.1:n.1109C>T
ENST00000644120.1:n.1935C>T
ENST00000644650.1:c.641C>T
ENST00000644905.1:n.1634C>T
ENST00000644969.2:c.1665C>T MANE Plus Clinical	ENSP00000496776.1:p.Leu555=
ENST00000646730.1:c.1545C>T	ENSP00000494784.1:p.Leu515=
ENST00000646891.1:c.1545C>T	ENSP00000493543.1:p.Leu515=
ENST00000647434.1:c.588C>T	ENSP00000495132.1:p.Leu196=
ENST00000288602.10:c.1545C>T	ENSP00000288602.6:p.Leu515=
ENST00000496384.6:c.368C>T
ENST00000497784.1:c.1580C>T	ENSP00000420119.1:n.1580C>T
NM_004333.4:c.1545C>T , LRG_299t1:c.1545C>T	NP_004324.2:p.Leu515=
XM_005250045.1:c.1545C>T	XP_005250102.1:p.Leu515=
XM_005250046.1:c.1545C>T	XP_005250103.1:p.Leu515=
XM_011516529.1:c.1545C>T	XP_011514831.1:p.Leu515=
XM_011516530.1:c.1545C>T	XP_011514832.1:p.Leu515=
XR_242190.1:n.1553C>T
XR_927520.1:n.1553C>T
XR_927521.1:n.1553C>T
XR_927522.1:n.1553C>T
XR_927523.1:n.1553C>T
NM_001354609.1:c.1545C>T	NP_001341538.1:p.Leu515=
NM_004333.5:c.1545C>T	NP_004324.2:p.Leu515=
NR_148928.1:n.1850C>T
XM_017012558.1:c.1665C>T	XP_016868047.1:p.Leu555=
XM_017012559.1:c.1665C>T	XP_016868048.1:p.Leu555=
XR_001744857.1:n.1673C>T
XR_001744858.1:n.1673C>T
NM_001354609.2:c.1545C>T	NP_001341538.1:p.Leu515=
NM_001374244.1:c.1665C>T	NP_001361173.1:p.Leu555=
NM_001374258.1:c.1665C>T MANE Plus Clinical	NP_001361187.1:p.Leu555=
NM_004333.6:c.1545C>T MANE Select	NP_004324.2:p.Leu515=
NM_001378467.1:c.1554C>T	NP_001365396.1:p.Leu518=
NM_001378468.1:c.1545C>T	NP_001365397.1:p.Leu515=
NM_001378469.1:c.1479C>T	NP_001365398.1:p.Leu493=
NM_001378470.1:c.1443C>T	NP_001365399.1:p.Leu481=
NM_001378471.1:c.1434C>T	NP_001365400.1:p.Leu478=
NM_001378472.1:c.1389C>T	NP_001365401.1:p.Leu463=
NM_001378473.1:c.1389C>T	NP_001365402.1:p.Leu463=
NM_001378474.1:c.1545C>T	NP_001365403.1:p.Leu515=
NM_001378475.1:c.1281C>T	NP_001365404.1:p.Leu427=