Canonical Allele Identifier: CA457986863

Gene: BRAF

Linked Data

• dbSNP Id: rs2128998202
• MyVariant Identifiers: chr7:g.140453111A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140753311A>G , CM000669.2:g.140753311A>G	GRCh38
NC_000007.13:g.140453111A>G , CM000669.1:g.140453111A>G	GRCh37
NC_000007.12:g.140099580A>G	NCBI36
NG_007873.3:g.176454T>C , LRG_299:g.176454T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.1824T>C MANE Select	ENSP00000493543.1:p.His608=
ENST00000288602.11:c.1944T>C	ENSP00000288602.7:p.His648=
ENST00000479537.6:c.494T>C
ENST00000496384.7:c.1824T>C	ENSP00000419060.2:p.His608=
ENST00000497784.2:c.*1274T>C	ENSP00000420119.2:n.*1274T>C
ENST00000642228.1:c.*902T>C	ENSP00000493678.1:n.*902T>C
ENST00000642875.1:n.1259-3893T>C
ENST00000644120.1:n.2214T>C
ENST00000644650.1:c.920T>C
ENST00000644905.1:n.2706T>C
ENST00000644969.2:c.1944T>C MANE Plus Clinical	ENSP00000496776.1:p.His648=
ENST00000646730.1:c.*400T>C	ENSP00000494784.1:n.*400T>C
ENST00000646891.1:c.1824T>C	ENSP00000493543.1:p.His608=
ENST00000647434.1:c.738-3893T>C	ENSP00000495132.1:n.738-3893T>C
ENST00000288602.10:c.1824T>C	ENSP00000288602.6:p.His608=
ENST00000479537.5:c.108T>C	ENSP00000418033.1:p.His36=
ENST00000496384.6:c.647T>C
ENST00000497784.1:c.1859T>C	ENSP00000420119.1:n.1859T>C
NM_004333.4:c.1824T>C , LRG_299t1:c.1824T>C	NP_004324.2:p.His608=
XM_005250045.1:c.1824T>C	XP_005250102.1:p.His608=
XM_005250046.1:c.1824T>C	XP_005250103.1:p.His608=
XM_011516529.1:c.1824T>C	XP_011514831.1:p.His608=
XM_011516530.1:c.1695-3893T>C	XP_011514832.1:n.1695-3893T>C
XR_242190.1:n.1832T>C
XR_927520.1:n.1832T>C
XR_927521.1:n.1832T>C
XR_927522.1:n.1703-3893T>C
XR_927523.1:n.1703-3893T>C
NM_001354609.1:c.1824T>C	NP_001341538.1:p.His608=
NM_004333.5:c.1824T>C	NP_004324.2:p.His608=
NR_148928.1:n.2922T>C
XM_017012558.1:c.1944T>C	XP_016868047.1:p.His648=
XM_017012559.1:c.1944T>C	XP_016868048.1:p.His648=
XR_001744857.1:n.1952T>C
XR_001744858.1:n.1823-3893T>C
NM_001354609.2:c.1824T>C	NP_001341538.1:p.His608=
NM_001374244.1:c.1944T>C	NP_001361173.1:p.His648=
NM_001374258.1:c.1944T>C MANE Plus Clinical	NP_001361187.1:p.His648=
NM_004333.6:c.1824T>C MANE Select	NP_004324.2:p.His608=
NM_001378467.1:c.1833T>C	NP_001365396.1:p.His611=
NM_001378468.1:c.1824T>C	NP_001365397.1:p.His608=
NM_001378469.1:c.1758T>C	NP_001365398.1:p.His586=
NM_001378470.1:c.1722T>C	NP_001365399.1:p.His574=
NM_001378471.1:c.1713T>C	NP_001365400.1:p.His571=
NM_001378472.1:c.1668T>C	NP_001365401.1:p.His556=
NM_001378473.1:c.1668T>C	NP_001365402.1:p.His556=
NM_001378474.1:c.1824T>C	NP_001365403.1:p.His608=
NM_001378475.1:c.1560T>C	NP_001365404.1:p.His520=