Canonical Allele Identifier: CA1747726093

Gene: BRAF

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140777240_140777241delinsCT , CM000669.2:g.140777240_140777241delinsCT	GRCh38
NC_000007.13:g.140477040_140477041delinsCT , CM000669.1:g.140477040_140477041delinsCT	GRCh37
NC_000007.12:g.140123509_140123510delinsCT	NCBI36
NG_007873.3:g.152524_152525delinsAG , LRG_299:g.152524_152525delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000646891.2:c.1518-153_1518-152delinsAG MANE Select	ENSP00000493543.1:n.1518-153_1518-152delinsAG
ENST00000288602.11:c.1638-153_1638-152delinsAG	ENSP00000288602.7:n.1638-153_1638-152delinsAG
ENST00000479537.6:c.188-153_188-152delinsAG
ENST00000496384.7:c.1518-153_1518-152delinsAG	ENSP00000419060.2:n.1518-153_1518-152delinsAG
ENST00000497784.2:c.*968-153_*968-152delinsAG	ENSP00000420119.2:n.*968-153_*968-152delinsAG
ENST00000642228.1:c.*596-153_*596-152delinsAG	ENSP00000493678.1:n.*596-153_*596-152delinsAG
ENST00000642875.1:n.1082-153_1082-152delinsAG
ENST00000644120.1:n.1908-153_1908-152delinsAG
ENST00000644650.1:c.614-153_614-152delinsAG
ENST00000644905.1:n.1607-153_1607-152delinsAG
ENST00000644969.2:c.1638-153_1638-152delinsAG MANE Plus Clinical	ENSP00000496776.1:n.1638-153_1638-152delinsAG
ENST00000646730.1:c.1518-153_1518-152delinsAG	ENSP00000494784.1:n.1518-153_1518-152delinsAG
ENST00000646891.1:c.1518-153_1518-152delinsAG	ENSP00000493543.1:n.1518-153_1518-152delinsAG
ENST00000647434.1:c.561-153_561-152delinsAG	ENSP00000495132.1:n.561-153_561-152delinsAG
ENST00000288602.10:c.1518-153_1518-152delinsAG	ENSP00000288602.6:n.1518-153_1518-152delinsAG
ENST00000496384.6:c.341-153_341-152delinsAG
ENST00000497784.1:c.1553-153_1553-152delinsAG	ENSP00000420119.1:n.1553-153_1553-152delinsAG
NM_004333.4:c.1518-153_1518-152delinsAG , LRG_299t1:c.1518-153_1518-152delinsAG	NP_004324.2:n.1518-153_1518-152delinsAG
XM_005250045.1:c.1518-153_1518-152delinsAG	XP_005250102.1:n.1518-153_1518-152delinsAG
XM_005250046.1:c.1518-153_1518-152delinsAG	XP_005250103.1:n.1518-153_1518-152delinsAG
XM_011516529.1:c.1518-153_1518-152delinsAG	XP_011514831.1:n.1518-153_1518-152delinsAG
XM_011516530.1:c.1518-153_1518-152delinsAG	XP_011514832.1:n.1518-153_1518-152delinsAG
XR_242190.1:n.1526-153_1526-152delinsAG
XR_927520.1:n.1526-153_1526-152delinsAG
XR_927521.1:n.1526-153_1526-152delinsAG
XR_927522.1:n.1526-153_1526-152delinsAG
XR_927523.1:n.1526-153_1526-152delinsAG
NM_001354609.1:c.1518-153_1518-152delinsAG	NP_001341538.1:n.1518-153_1518-152delinsAG
NM_004333.5:c.1518-153_1518-152delinsAG	NP_004324.2:n.1518-153_1518-152delinsAG
NR_148928.1:n.1823-153_1823-152delinsAG
XM_017012558.1:c.1638-153_1638-152delinsAG	XP_016868047.1:n.1638-153_1638-152delinsAG
XM_017012559.1:c.1638-153_1638-152delinsAG	XP_016868048.1:n.1638-153_1638-152delinsAG
XR_001744857.1:n.1646-153_1646-152delinsAG
XR_001744858.1:n.1646-153_1646-152delinsAG
NM_001354609.2:c.1518-153_1518-152delinsAG	NP_001341538.1:n.1518-153_1518-152delinsAG
NM_001374244.1:c.1638-153_1638-152delinsAG	NP_001361173.1:n.1638-153_1638-152delinsAG
NM_001374258.1:c.1638-153_1638-152delinsAG MANE Plus Clinical	NP_001361187.1:n.1638-153_1638-152delinsAG
NM_004333.6:c.1518-153_1518-152delinsAG MANE Select	NP_004324.2:n.1518-153_1518-152delinsAG
NM_001378467.1:c.1527-153_1527-152delinsAG	NP_001365396.1:n.1527-153_1527-152delinsAG
NM_001378468.1:c.1518-153_1518-152delinsAG	NP_001365397.1:n.1518-153_1518-152delinsAG
NM_001378469.1:c.1452-153_1452-152delinsAG	NP_001365398.1:n.1452-153_1452-152delinsAG
NM_001378470.1:c.1416-153_1416-152delinsAG	NP_001365399.1:n.1416-153_1416-152delinsAG
NM_001378471.1:c.1407-153_1407-152delinsAG	NP_001365400.1:n.1407-153_1407-152delinsAG
NM_001378472.1:c.1362-153_1362-152delinsAG	NP_001365401.1:n.1362-153_1362-152delinsAG
NM_001378473.1:c.1362-153_1362-152delinsAG	NP_001365402.1:n.1362-153_1362-152delinsAG
NM_001378474.1:c.1518-153_1518-152delinsAG	NP_001365403.1:n.1518-153_1518-152delinsAG
NM_001378475.1:c.1254-153_1254-152delinsAG	NP_001365404.1:n.1254-153_1254-152delinsAG