Canonical Allele Identifier: CA457986836
Gene: BRAF HGNC NCBI

Linked Data

dbSNP Id: rs2128998163
MyVariant Identifiers: chr7:g.140453099C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140753299C>T , CM000669.2:g.140753299C>T GRCh38
NC_000007.13:g.140453099C>T , CM000669.1:g.140453099C>T GRCh37
NC_000007.12:g.140099568C>T NCBI36
NG_007873.3:g.176466G>A , LRG_299:g.176466G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000646891.2:c.1836G>A MANE Select ENSP00000493543.1:p.Gln612=
ENST00000288602.11:c.1956G>A ENSP00000288602.7:p.Gln652=
ENST00000479537.6:c.506G>A
ENST00000496384.7:c.1836G>A ENSP00000419060.2:p.Gln612=
ENST00000497784.2:c.*1286G>A ENSP00000420119.2:n.*1286G>A
ENST00000642228.1:c.*914G>A ENSP00000493678.1:n.*914G>A
ENST00000642875.1:n.1259-3881G>A
ENST00000644120.1:n.2226G>A
ENST00000644650.1:c.932G>A
ENST00000644905.1:n.2718G>A
ENST00000644969.2:c.1956G>A MANE Plus Clinical ENSP00000496776.1:p.Gln652=
ENST00000646730.1:c.*412G>A ENSP00000494784.1:n.*412G>A
ENST00000646891.1:c.1836G>A ENSP00000493543.1:p.Gln612=
ENST00000647434.1:c.738-3881G>A ENSP00000495132.1:n.738-3881G>A
ENST00000288602.10:c.1836G>A ENSP00000288602.6:p.Gln612=
ENST00000479537.5:c.120G>A ENSP00000418033.1:p.Gln40=
ENST00000496384.6:c.659G>A
ENST00000497784.1:c.1871G>A ENSP00000420119.1:n.1871G>A
NM_004333.4:c.1836G>A , LRG_299t1:c.1836G>A NP_004324.2:p.Gln612=
XM_005250045.1:c.1836G>A XP_005250102.1:p.Gln612=
XM_005250046.1:c.1836G>A XP_005250103.1:p.Gln612=
XM_011516529.1:c.1836G>A XP_011514831.1:p.Gln612=
XM_011516530.1:c.1695-3881G>A XP_011514832.1:n.1695-3881G>A
XR_242190.1:n.1844G>A
XR_927520.1:n.1844G>A
XR_927521.1:n.1844G>A
XR_927522.1:n.1703-3881G>A
XR_927523.1:n.1703-3881G>A
NM_001354609.1:c.1836G>A NP_001341538.1:p.Gln612=
NM_004333.5:c.1836G>A NP_004324.2:p.Gln612=
NR_148928.1:n.2934G>A
XM_017012558.1:c.1956G>A XP_016868047.1:p.Gln652=
XM_017012559.1:c.1956G>A XP_016868048.1:p.Gln652=
XR_001744857.1:n.1964G>A
XR_001744858.1:n.1823-3881G>A
NM_001354609.2:c.1836G>A NP_001341538.1:p.Gln612=
NM_001374244.1:c.1956G>A NP_001361173.1:p.Gln652=
NM_001374258.1:c.1956G>A MANE Plus Clinical NP_001361187.1:p.Gln652=
NM_004333.6:c.1836G>A MANE Select NP_004324.2:p.Gln612=
NM_001378467.1:c.1845G>A NP_001365396.1:p.Gln615=
NM_001378468.1:c.1836G>A NP_001365397.1:p.Gln612=
NM_001378469.1:c.1770G>A NP_001365398.1:p.Gln590=
NM_001378470.1:c.1734G>A NP_001365399.1:p.Gln578=
NM_001378471.1:c.1725G>A NP_001365400.1:p.Gln575=
NM_001378472.1:c.1680G>A NP_001365401.1:p.Gln560=
NM_001378473.1:c.1680G>A NP_001365402.1:p.Gln560=
NM_001378474.1:c.1836G>A NP_001365403.1:p.Gln612=
NM_001378475.1:c.1572G>A NP_001365404.1:p.Gln524=