Canonical Allele Identifier: CA834225059

Gene: BRAF

Linked Data

• dbSNP Id: rs1280233167
• gnomAD v3: 7-140777373-T-A
• gnomAD v4: 7-140777373-T-A
• MyVariant Identifiers: chr7:g.140477173T>A (hg19) ; chr7:g.140777373T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140777373T>A , CM000669.2:g.140777373T>A	GRCh38
NC_000007.13:g.140477173T>A , CM000669.1:g.140477173T>A	GRCh37
NC_000007.12:g.140123642T>A	NCBI36
NG_007873.3:g.152392A>T , LRG_299:g.152392A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1518-285A>T MANE Select	ENSP00000493543.1:n.1518-285A>T
ENST00000288602.11:c.1638-285A>T	ENSP00000288602.7:n.1638-285A>T
ENST00000479537.6:c.188-285A>T
ENST00000496384.7:c.1518-285A>T	ENSP00000419060.2:n.1518-285A>T
ENST00000497784.2:c.*968-285A>T	ENSP00000420119.2:n.*968-285A>T
ENST00000642228.1:c.*596-285A>T	ENSP00000493678.1:n.*596-285A>T
ENST00000642875.1:n.1082-285A>T
ENST00000644120.1:n.1908-285A>T
ENST00000644650.1:c.614-285A>T
ENST00000644905.1:n.1607-285A>T
ENST00000644969.2:c.1638-285A>T MANE Plus Clinical	ENSP00000496776.1:n.1638-285A>T
ENST00000646730.1:c.1518-285A>T	ENSP00000494784.1:n.1518-285A>T
ENST00000646891.1:c.1518-285A>T	ENSP00000493543.1:n.1518-285A>T
ENST00000647434.1:c.561-285A>T	ENSP00000495132.1:n.561-285A>T
ENST00000288602.10:c.1518-285A>T	ENSP00000288602.6:n.1518-285A>T
ENST00000496384.6:c.341-285A>T
ENST00000497784.1:c.1553-285A>T	ENSP00000420119.1:n.1553-285A>T
NM_004333.4:c.1518-285A>T , LRG_299t1:c.1518-285A>T	NP_004324.2:n.1518-285A>T
XM_005250045.1:c.1518-285A>T	XP_005250102.1:n.1518-285A>T
XM_005250046.1:c.1518-285A>T	XP_005250103.1:n.1518-285A>T
XM_011516529.1:c.1518-285A>T	XP_011514831.1:n.1518-285A>T
XM_011516530.1:c.1518-285A>T	XP_011514832.1:n.1518-285A>T
XR_242190.1:n.1526-285A>T
XR_927520.1:n.1526-285A>T
XR_927521.1:n.1526-285A>T
XR_927522.1:n.1526-285A>T
XR_927523.1:n.1526-285A>T
NM_001354609.1:c.1518-285A>T	NP_001341538.1:n.1518-285A>T
NM_004333.5:c.1518-285A>T	NP_004324.2:n.1518-285A>T
NR_148928.1:n.1823-285A>T
XM_017012558.1:c.1638-285A>T	XP_016868047.1:n.1638-285A>T
XM_017012559.1:c.1638-285A>T	XP_016868048.1:n.1638-285A>T
XR_001744857.1:n.1646-285A>T
XR_001744858.1:n.1646-285A>T
NM_001354609.2:c.1518-285A>T	NP_001341538.1:n.1518-285A>T
NM_001374244.1:c.1638-285A>T	NP_001361173.1:n.1638-285A>T
NM_001374258.1:c.1638-285A>T MANE Plus Clinical	NP_001361187.1:n.1638-285A>T
NM_004333.6:c.1518-285A>T MANE Select	NP_004324.2:n.1518-285A>T
NM_001378467.1:c.1527-285A>T	NP_001365396.1:n.1527-285A>T
NM_001378468.1:c.1518-285A>T	NP_001365397.1:n.1518-285A>T
NM_001378469.1:c.1452-285A>T	NP_001365398.1:n.1452-285A>T
NM_001378470.1:c.1416-285A>T	NP_001365399.1:n.1416-285A>T
NM_001378471.1:c.1407-285A>T	NP_001365400.1:n.1407-285A>T
NM_001378472.1:c.1362-285A>T	NP_001365401.1:n.1362-285A>T
NM_001378473.1:c.1362-285A>T	NP_001365402.1:n.1362-285A>T
NM_001378474.1:c.1518-285A>T	NP_001365403.1:n.1518-285A>T
NM_001378475.1:c.1254-285A>T	NP_001365404.1:n.1254-285A>T