Canonical Allele Identifier: CA369543303

Gene: BRAF

Linked Data

• dbSNP Id: rs2128998461
• MyVariant Identifiers: chr7:g.140453180A>T (hg19) ; chr7:g.140753380A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140753380A>T , CM000669.2:g.140753380A>T	GRCh38
NC_000007.13:g.140453180A>T , CM000669.1:g.140453180A>T	GRCh37
NC_000007.12:g.140099649A>T	NCBI36
NG_007873.3:g.176385T>A , LRG_299:g.176385T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.1755T>A MANE Select	ENSP00000493543.1:p.His585Gln
ENST00000288602.11:c.1875T>A	ENSP00000288602.7:p.His625Gln
ENST00000479537.6:c.425T>A
ENST00000496384.7:c.1755T>A	ENSP00000419060.2:p.His585Gln
ENST00000497784.2:c.*1205T>A	ENSP00000420119.2:n.*1205T>A
ENST00000642228.1:c.*833T>A	ENSP00000493678.1:n.*833T>A
ENST00000642875.1:n.1259-3962T>A
ENST00000644120.1:n.2145T>A
ENST00000644650.1:c.851T>A
ENST00000644905.1:n.2637T>A
ENST00000644969.2:c.1875T>A MANE Plus Clinical	ENSP00000496776.1:p.His625Gln
ENST00000646730.1:c.*331T>A	ENSP00000494784.1:n.*331T>A
ENST00000646891.1:c.1755T>A	ENSP00000493543.1:p.His585Gln
ENST00000647434.1:c.738-3962T>A	ENSP00000495132.1:n.738-3962T>A
ENST00000288602.10:c.1755T>A	ENSP00000288602.6:p.His585Gln
ENST00000479537.5:c.39T>A	ENSP00000418033.1:p.His13Gln
ENST00000496384.6:c.578T>A
ENST00000497784.1:c.1790T>A	ENSP00000420119.1:n.1790T>A
NM_004333.4:c.1755T>A , LRG_299t1:c.1755T>A	NP_004324.2:p.His585Gln
XM_005250045.1:c.1755T>A	XP_005250102.1:p.His585Gln
XM_005250046.1:c.1755T>A	XP_005250103.1:p.His585Gln
XM_011516529.1:c.1755T>A	XP_011514831.1:p.His585Gln
XM_011516530.1:c.1695-3962T>A	XP_011514832.1:n.1695-3962T>A
XR_242190.1:n.1763T>A
XR_927520.1:n.1763T>A
XR_927521.1:n.1763T>A
XR_927522.1:n.1703-3962T>A
XR_927523.1:n.1703-3962T>A
NM_001354609.1:c.1755T>A	NP_001341538.1:p.His585Gln
NM_004333.5:c.1755T>A	NP_004324.2:p.His585Gln
NR_148928.1:n.2853T>A
XM_017012558.1:c.1875T>A	XP_016868047.1:p.His625Gln
XM_017012559.1:c.1875T>A	XP_016868048.1:p.His625Gln
XR_001744857.1:n.1883T>A
XR_001744858.1:n.1823-3962T>A
NM_001354609.2:c.1755T>A	NP_001341538.1:p.His585Gln
NM_001374244.1:c.1875T>A	NP_001361173.1:p.His625Gln
NM_001374258.1:c.1875T>A MANE Plus Clinical	NP_001361187.1:p.His625Gln
NM_004333.6:c.1755T>A MANE Select	NP_004324.2:p.His585Gln
NM_001378467.1:c.1764T>A	NP_001365396.1:p.His588Gln
NM_001378468.1:c.1755T>A	NP_001365397.1:p.His585Gln
NM_001378469.1:c.1689T>A	NP_001365398.1:p.His563Gln
NM_001378470.1:c.1653T>A	NP_001365399.1:p.His551Gln
NM_001378471.1:c.1644T>A	NP_001365400.1:p.His548Gln
NM_001378472.1:c.1599T>A	NP_001365401.1:p.His533Gln
NM_001378473.1:c.1599T>A	NP_001365402.1:p.His533Gln
NM_001378474.1:c.1755T>A	NP_001365403.1:p.His585Gln
NM_001378475.1:c.1491T>A	NP_001365404.1:p.His497Gln