Canonical Allele Identifier: CA457987534
Gene: BRAF HGNC NCBI

Linked Data

dbSNP Id: rs2128999629
MyVariant Identifiers: chr7:g.140454009G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140754209G>A , CM000669.2:g.140754209G>A GRCh38
NC_000007.13:g.140454009G>A , CM000669.1:g.140454009G>A GRCh37
NC_000007.12:g.140100478G>A NCBI36
NG_007873.3:g.175556C>T , LRG_299:g.175556C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000646891.2:c.1719C>T MANE Select ENSP00000493543.1:p.Ile573=
ENST00000288602.11:c.1839C>T ENSP00000288602.7:p.Ile613=
ENST00000479537.6:c.389C>T
ENST00000496384.7:c.1719C>T ENSP00000419060.2:p.Ile573=
ENST00000497784.2:c.*1169C>T ENSP00000420119.2:n.*1169C>T
ENST00000642228.1:c.*797C>T ENSP00000493678.1:n.*797C>T
ENST00000642875.1:n.1259-4791C>T
ENST00000644120.1:n.2109C>T
ENST00000644650.1:c.815C>T
ENST00000644905.1:n.1808C>T
ENST00000644969.2:c.1839C>T MANE Plus Clinical ENSP00000496776.1:p.Ile613=
ENST00000646730.1:c.*295C>T ENSP00000494784.1:n.*295C>T
ENST00000646891.1:c.1719C>T ENSP00000493543.1:p.Ile573=
ENST00000647434.1:c.738-4791C>T ENSP00000495132.1:n.738-4791C>T
ENST00000288602.10:c.1719C>T ENSP00000288602.6:p.Ile573=
ENST00000479537.5:c.3C>T ENSP00000418033.1:p.Ile1=
ENST00000496384.6:c.542C>T
ENST00000497784.1:c.1754C>T ENSP00000420119.1:n.1754C>T
NM_004333.4:c.1719C>T , LRG_299t1:c.1719C>T NP_004324.2:p.Ile573=
XM_005250045.1:c.1719C>T XP_005250102.1:p.Ile573=
XM_005250046.1:c.1719C>T XP_005250103.1:p.Ile573=
XM_011516529.1:c.1719C>T XP_011514831.1:p.Ile573=
XM_011516530.1:c.1695-4791C>T XP_011514832.1:n.1695-4791C>T
XR_242190.1:n.1727C>T
XR_927520.1:n.1727C>T
XR_927521.1:n.1727C>T
XR_927522.1:n.1703-4791C>T
XR_927523.1:n.1703-4791C>T
NM_001354609.1:c.1719C>T NP_001341538.1:p.Ile573=
NM_004333.5:c.1719C>T NP_004324.2:p.Ile573=
NR_148928.1:n.2024C>T
XM_017012558.1:c.1839C>T XP_016868047.1:p.Ile613=
XM_017012559.1:c.1839C>T XP_016868048.1:p.Ile613=
XR_001744857.1:n.1847C>T
XR_001744858.1:n.1823-4791C>T
NM_001354609.2:c.1719C>T NP_001341538.1:p.Ile573=
NM_001374244.1:c.1839C>T NP_001361173.1:p.Ile613=
NM_001374258.1:c.1839C>T MANE Plus Clinical NP_001361187.1:p.Ile613=
NM_004333.6:c.1719C>T MANE Select NP_004324.2:p.Ile573=
NM_001378467.1:c.1728C>T NP_001365396.1:p.Ile576=
NM_001378468.1:c.1719C>T NP_001365397.1:p.Ile573=
NM_001378469.1:c.1653C>T NP_001365398.1:p.Ile551=
NM_001378470.1:c.1617C>T NP_001365399.1:p.Ile539=
NM_001378471.1:c.1608C>T NP_001365400.1:p.Ile536=
NM_001378472.1:c.1563C>T NP_001365401.1:p.Ile521=
NM_001378473.1:c.1563C>T NP_001365402.1:p.Ile521=
NM_001378474.1:c.1719C>T NP_001365403.1:p.Ile573=
NM_001378475.1:c.1455C>T NP_001365404.1:p.Ile485=