Canonical Allele Identifier: CA1747726152

Gene: BRAF

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140777395_140777396delinsAT , CM000669.2:g.140777395_140777396delinsAT	GRCh38
NC_000007.13:g.140477195_140477196delinsAT , CM000669.1:g.140477195_140477196delinsAT	GRCh37
NC_000007.12:g.140123664_140123665delinsAT	NCBI36
NG_007873.3:g.152369_152370delinsAT , LRG_299:g.152369_152370delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1518-308_1518-307delinsAT MANE Select	ENSP00000493543.1:n.1518-308_1518-307delinsAT
ENST00000288602.11:c.1638-308_1638-307delinsAT	ENSP00000288602.7:n.1638-308_1638-307delinsAT
ENST00000479537.6:c.188-308_188-307delinsAT
ENST00000496384.7:c.1518-308_1518-307delinsAT	ENSP00000419060.2:n.1518-308_1518-307delinsAT
ENST00000497784.2:c.*968-308_*968-307delinsAT	ENSP00000420119.2:n.*968-308_*968-307delinsAT
ENST00000642228.1:c.*596-308_*596-307delinsAT	ENSP00000493678.1:n.*596-308_*596-307delinsAT
ENST00000642875.1:n.1082-308_1082-307delinsAT
ENST00000644120.1:n.1908-308_1908-307delinsAT
ENST00000644650.1:c.614-308_614-307delinsAT
ENST00000644905.1:n.1607-308_1607-307delinsAT
ENST00000644969.2:c.1638-308_1638-307delinsAT MANE Plus Clinical	ENSP00000496776.1:n.1638-308_1638-307delinsAT
ENST00000646730.1:c.1518-308_1518-307delinsAT	ENSP00000494784.1:n.1518-308_1518-307delinsAT
ENST00000646891.1:c.1518-308_1518-307delinsAT	ENSP00000493543.1:n.1518-308_1518-307delinsAT
ENST00000647434.1:c.561-308_561-307delinsAT	ENSP00000495132.1:n.561-308_561-307delinsAT
ENST00000288602.10:c.1518-308_1518-307delinsAT	ENSP00000288602.6:n.1518-308_1518-307delinsAT
ENST00000496384.6:c.341-308_341-307delinsAT
ENST00000497784.1:c.1553-308_1553-307delinsAT	ENSP00000420119.1:n.1553-308_1553-307delinsAT
NM_004333.4:c.1518-308_1518-307delinsAT , LRG_299t1:c.1518-308_1518-307delinsAT	NP_004324.2:n.1518-308_1518-307delinsAT
XM_005250045.1:c.1518-308_1518-307delinsAT	XP_005250102.1:n.1518-308_1518-307delinsAT
XM_005250046.1:c.1518-308_1518-307delinsAT	XP_005250103.1:n.1518-308_1518-307delinsAT
XM_011516529.1:c.1518-308_1518-307delinsAT	XP_011514831.1:n.1518-308_1518-307delinsAT
XM_011516530.1:c.1518-308_1518-307delinsAT	XP_011514832.1:n.1518-308_1518-307delinsAT
XR_242190.1:n.1526-308_1526-307delinsAT
XR_927520.1:n.1526-308_1526-307delinsAT
XR_927521.1:n.1526-308_1526-307delinsAT
XR_927522.1:n.1526-308_1526-307delinsAT
XR_927523.1:n.1526-308_1526-307delinsAT
NM_001354609.1:c.1518-308_1518-307delinsAT	NP_001341538.1:n.1518-308_1518-307delinsAT
NM_004333.5:c.1518-308_1518-307delinsAT	NP_004324.2:n.1518-308_1518-307delinsAT
NR_148928.1:n.1823-308_1823-307delinsAT
XM_017012558.1:c.1638-308_1638-307delinsAT	XP_016868047.1:n.1638-308_1638-307delinsAT
XM_017012559.1:c.1638-308_1638-307delinsAT	XP_016868048.1:n.1638-308_1638-307delinsAT
XR_001744857.1:n.1646-308_1646-307delinsAT
XR_001744858.1:n.1646-308_1646-307delinsAT
NM_001354609.2:c.1518-308_1518-307delinsAT	NP_001341538.1:n.1518-308_1518-307delinsAT
NM_001374244.1:c.1638-308_1638-307delinsAT	NP_001361173.1:n.1638-308_1638-307delinsAT
NM_001374258.1:c.1638-308_1638-307delinsAT MANE Plus Clinical	NP_001361187.1:n.1638-308_1638-307delinsAT
NM_004333.6:c.1518-308_1518-307delinsAT MANE Select	NP_004324.2:n.1518-308_1518-307delinsAT
NM_001378467.1:c.1527-308_1527-307delinsAT	NP_001365396.1:n.1527-308_1527-307delinsAT
NM_001378468.1:c.1518-308_1518-307delinsAT	NP_001365397.1:n.1518-308_1518-307delinsAT
NM_001378469.1:c.1452-308_1452-307delinsAT	NP_001365398.1:n.1452-308_1452-307delinsAT
NM_001378470.1:c.1416-308_1416-307delinsAT	NP_001365399.1:n.1416-308_1416-307delinsAT
NM_001378471.1:c.1407-308_1407-307delinsAT	NP_001365400.1:n.1407-308_1407-307delinsAT
NM_001378472.1:c.1362-308_1362-307delinsAT	NP_001365401.1:n.1362-308_1362-307delinsAT
NM_001378473.1:c.1362-308_1362-307delinsAT	NP_001365402.1:n.1362-308_1362-307delinsAT
NM_001378474.1:c.1518-308_1518-307delinsAT	NP_001365403.1:n.1518-308_1518-307delinsAT
NM_001378475.1:c.1254-308_1254-307delinsAT	NP_001365404.1:n.1254-308_1254-307delinsAT