Canonical Allele Identifier: CA369543951

Gene: BRAF

Linked Data

• MyVariant Identifiers: chr7:g.140454019T>G (hg19) ; chr7:g.140754219T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140754219T>G , CM000669.2:g.140754219T>G	GRCh38
NC_000007.13:g.140454019T>G , CM000669.1:g.140454019T>G	GRCh37
NC_000007.12:g.140100488T>G	NCBI36
NG_007873.3:g.175546A>C , LRG_299:g.175546A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.1709A>C MANE Select	ENSP00000493543.1:p.Lys570Thr
ENST00000288602.11:c.1829A>C	ENSP00000288602.7:p.Lys610Thr
ENST00000479537.6:c.379A>C
ENST00000496384.7:c.1709A>C	ENSP00000419060.2:p.Lys570Thr
ENST00000497784.2:c.*1159A>C	ENSP00000420119.2:n.*1159A>C
ENST00000642228.1:c.*787A>C	ENSP00000493678.1:n.*787A>C
ENST00000642875.1:n.1259-4801A>C
ENST00000644120.1:n.2099A>C
ENST00000644650.1:c.805A>C
ENST00000644905.1:n.1798A>C
ENST00000644969.2:c.1829A>C MANE Plus Clinical	ENSP00000496776.1:p.Lys610Thr
ENST00000646730.1:c.*285A>C	ENSP00000494784.1:n.*285A>C
ENST00000646891.1:c.1709A>C	ENSP00000493543.1:p.Lys570Thr
ENST00000647434.1:c.738-4801A>C	ENSP00000495132.1:n.738-4801A>C
ENST00000288602.10:c.1709A>C	ENSP00000288602.6:p.Lys570Thr
ENST00000496384.6:c.532A>C
ENST00000497784.1:c.1744A>C	ENSP00000420119.1:n.1744A>C
NM_004333.4:c.1709A>C , LRG_299t1:c.1709A>C	NP_004324.2:p.Lys570Thr
XM_005250045.1:c.1709A>C	XP_005250102.1:p.Lys570Thr
XM_005250046.1:c.1709A>C	XP_005250103.1:p.Lys570Thr
XM_011516529.1:c.1709A>C	XP_011514831.1:p.Lys570Thr
XM_011516530.1:c.1695-4801A>C	XP_011514832.1:n.1695-4801A>C
XR_242190.1:n.1717A>C
XR_927520.1:n.1717A>C
XR_927521.1:n.1717A>C
XR_927522.1:n.1703-4801A>C
XR_927523.1:n.1703-4801A>C
NM_001354609.1:c.1709A>C	NP_001341538.1:p.Lys570Thr
NM_004333.5:c.1709A>C	NP_004324.2:p.Lys570Thr
NR_148928.1:n.2014A>C
XM_017012558.1:c.1829A>C	XP_016868047.1:p.Lys610Thr
XM_017012559.1:c.1829A>C	XP_016868048.1:p.Lys610Thr
XR_001744857.1:n.1837A>C
XR_001744858.1:n.1823-4801A>C
NM_001354609.2:c.1709A>C	NP_001341538.1:p.Lys570Thr
NM_001374244.1:c.1829A>C	NP_001361173.1:p.Lys610Thr
NM_001374258.1:c.1829A>C MANE Plus Clinical	NP_001361187.1:p.Lys610Thr
NM_004333.6:c.1709A>C MANE Select	NP_004324.2:p.Lys570Thr
NM_001378467.1:c.1718A>C	NP_001365396.1:p.Lys573Thr
NM_001378468.1:c.1709A>C	NP_001365397.1:p.Lys570Thr
NM_001378469.1:c.1643A>C	NP_001365398.1:p.Lys548Thr
NM_001378470.1:c.1607A>C	NP_001365399.1:p.Lys536Thr
NM_001378471.1:c.1598A>C	NP_001365400.1:p.Lys533Thr
NM_001378472.1:c.1553A>C	NP_001365401.1:p.Lys518Thr
NM_001378473.1:c.1553A>C	NP_001365402.1:p.Lys518Thr
NM_001378474.1:c.1709A>C	NP_001365403.1:p.Lys570Thr
NM_001378475.1:c.1445A>C	NP_001365404.1:p.Lys482Thr