Canonical Allele Identifier: CA2685241017

Gene: BRAF

Linked Data

• gnomAD v4: 7-140777203-TTTA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140777204_140777206del , CM000669.2:g.140777204_140777206del	GRCh38
NC_000007.13:g.140477004_140477006del , CM000669.1:g.140477004_140477006del	GRCh37
NC_000007.12:g.140123473_140123475del	NCBI36
NG_007873.3:g.152559_152561del , LRG_299:g.152559_152561del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1518-118_1518-116del MANE Select	ENSP00000493543.1:n.1518-118_1518-116del
ENST00000288602.11:c.1638-118_1638-116del	ENSP00000288602.7:n.1638-118_1638-116del
ENST00000479537.6:c.188-118_188-116del
ENST00000496384.7:c.1518-118_1518-116del	ENSP00000419060.2:n.1518-118_1518-116del
ENST00000497784.2:c.*968-118_*968-116del	ENSP00000420119.2:n.*968-118_*968-116del
ENST00000642228.1:c.*596-118_*596-116del	ENSP00000493678.1:n.*596-118_*596-116del
ENST00000642875.1:n.1082-118_1082-116del
ENST00000644120.1:n.1908-118_1908-116del
ENST00000644650.1:c.614-118_614-116del
ENST00000644905.1:n.1607-118_1607-116del
ENST00000644969.2:c.1638-118_1638-116del MANE Plus Clinical	ENSP00000496776.1:n.1638-118_1638-116del
ENST00000646730.1:c.1518-118_1518-116del	ENSP00000494784.1:n.1518-118_1518-116del
ENST00000646891.1:c.1518-118_1518-116del	ENSP00000493543.1:n.1518-118_1518-116del
ENST00000647434.1:c.561-118_561-116del	ENSP00000495132.1:n.561-118_561-116del
ENST00000288602.10:c.1518-118_1518-116del	ENSP00000288602.6:n.1518-118_1518-116del
ENST00000496384.6:c.341-118_341-116del
ENST00000497784.1:c.1553-118_1553-116del	ENSP00000420119.1:n.1553-118_1553-116del
NM_004333.4:c.1518-118_1518-116del , LRG_299t1:c.1518-118_1518-116del	NP_004324.2:n.1518-118_1518-116del
XM_005250045.1:c.1518-118_1518-116del	XP_005250102.1:n.1518-118_1518-116del
XM_005250046.1:c.1518-118_1518-116del	XP_005250103.1:n.1518-118_1518-116del
XM_011516529.1:c.1518-118_1518-116del	XP_011514831.1:n.1518-118_1518-116del
XM_011516530.1:c.1518-118_1518-116del	XP_011514832.1:n.1518-118_1518-116del
XR_242190.1:n.1526-118_1526-116del
XR_927520.1:n.1526-118_1526-116del
XR_927521.1:n.1526-118_1526-116del
XR_927522.1:n.1526-118_1526-116del
XR_927523.1:n.1526-118_1526-116del
NM_001354609.1:c.1518-118_1518-116del	NP_001341538.1:n.1518-118_1518-116del
NM_004333.5:c.1518-118_1518-116del	NP_004324.2:n.1518-118_1518-116del
NR_148928.1:n.1823-118_1823-116del
XM_017012558.1:c.1638-118_1638-116del	XP_016868047.1:n.1638-118_1638-116del
XM_017012559.1:c.1638-118_1638-116del	XP_016868048.1:n.1638-118_1638-116del
XR_001744857.1:n.1646-118_1646-116del
XR_001744858.1:n.1646-118_1646-116del
NM_001354609.2:c.1518-118_1518-116del	NP_001341538.1:n.1518-118_1518-116del
NM_001374244.1:c.1638-118_1638-116del	NP_001361173.1:n.1638-118_1638-116del
NM_001374258.1:c.1638-118_1638-116del MANE Plus Clinical	NP_001361187.1:n.1638-118_1638-116del
NM_004333.6:c.1518-118_1518-116del MANE Select	NP_004324.2:n.1518-118_1518-116del
NM_001378467.1:c.1527-118_1527-116del	NP_001365396.1:n.1527-118_1527-116del
NM_001378468.1:c.1518-118_1518-116del	NP_001365397.1:n.1518-118_1518-116del
NM_001378469.1:c.1452-118_1452-116del	NP_001365398.1:n.1452-118_1452-116del
NM_001378470.1:c.1416-118_1416-116del	NP_001365399.1:n.1416-118_1416-116del
NM_001378471.1:c.1407-118_1407-116del	NP_001365400.1:n.1407-118_1407-116del
NM_001378472.1:c.1362-118_1362-116del	NP_001365401.1:n.1362-118_1362-116del
NM_001378473.1:c.1362-118_1362-116del	NP_001365402.1:n.1362-118_1362-116del
NM_001378474.1:c.1518-118_1518-116del	NP_001365403.1:n.1518-118_1518-116del
NM_001378475.1:c.1254-118_1254-116del	NP_001365404.1:n.1254-118_1254-116del