Canonical Allele Identifier: CA1747714928

Gene: BRAF

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140777971_140777972delinsAG , CM000669.2:g.140777971_140777972delinsAG	GRCh38
NC_000007.13:g.140477771_140477772delinsAG , CM000669.1:g.140477771_140477772delinsAG	GRCh37
NC_000007.12:g.140124240_140124241delinsAG	NCBI36
NG_007873.3:g.151793_151794delinsCT , LRG_299:g.151793_151794delinsCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.1517+19_1517+20delinsCT MANE Select	ENSP00000493543.1:n.1517+19_1517+20delins...
ENST00000288602.11:c.1637+19_1637+20delinsCT	ENSP00000288602.7:n.1637+19_1637+20delins...
ENST00000479537.6:c.187+19_187+20delinsCT
ENST00000496384.7:c.1517+19_1517+20delinsCT	ENSP00000419060.2:n.1517+19_1517+20delins...
ENST00000497784.2:c.*967+19_*967+20delinsCT	ENSP00000420119.2:n.*967+19_*967+20delins...
ENST00000642228.1:c.*595+19_*595+20delinsCT	ENSP00000493678.1:n.*595+19_*595+20delins...
ENST00000642875.1:n.1081+19_1081+20delinsCT
ENST00000644120.1:n.1907+19_1907+20delinsCT
ENST00000644650.1:c.613+19_613+20delinsCT
ENST00000644905.1:n.1606+19_1606+20delinsCT
ENST00000644969.2:c.1637+19_1637+20delinsCT MANE Plus Clinical	ENSP00000496776.1:n.1637+19_1637+20delins...
ENST00000646730.1:c.1517+19_1517+20delinsCT	ENSP00000494784.1:n.1517+19_1517+20delins...
ENST00000646891.1:c.1517+19_1517+20delinsCT	ENSP00000493543.1:n.1517+19_1517+20delins...
ENST00000647434.1:c.560+19_560+20delinsCT	ENSP00000495132.1:n.560+19_560+20delinsCT...
ENST00000288602.10:c.1517+19_1517+20delinsCT	ENSP00000288602.6:n.1517+19_1517+20delins...
ENST00000496384.6:c.340+19_340+20delinsCT
ENST00000497784.1:c.1552+19_1552+20delinsCT	ENSP00000420119.1:n.1552+19_1552+20delins...
NM_004333.4:c.1517+19_1517+20delinsCT , LRG_299t1:c.1517+19_1517+20delinsCT	NP_004324.2:n.1517+19_1517+20delinsCT
XM_005250045.1:c.1517+19_1517+20delinsCT	XP_005250102.1:n.1517+19_1517+20delinsCT
XM_005250046.1:c.1517+19_1517+20delinsCT	XP_005250103.1:n.1517+19_1517+20delinsCT
XM_011516529.1:c.1517+19_1517+20delinsCT	XP_011514831.1:n.1517+19_1517+20delinsCT
XM_011516530.1:c.1517+19_1517+20delinsCT	XP_011514832.1:n.1517+19_1517+20delinsCT
XR_242190.1:n.1525+19_1525+20delinsCT
XR_927520.1:n.1525+19_1525+20delinsCT
XR_927521.1:n.1525+19_1525+20delinsCT
XR_927522.1:n.1525+19_1525+20delinsCT
XR_927523.1:n.1525+19_1525+20delinsCT
NM_001354609.1:c.1517+19_1517+20delinsCT	NP_001341538.1:n.1517+19_1517+20delinsCT
NM_004333.5:c.1517+19_1517+20delinsCT	NP_004324.2:n.1517+19_1517+20delinsCT
NR_148928.1:n.1822+19_1822+20delinsCT
XM_017012558.1:c.1637+19_1637+20delinsCT	XP_016868047.1:n.1637+19_1637+20delinsCT
XM_017012559.1:c.1637+19_1637+20delinsCT	XP_016868048.1:n.1637+19_1637+20delinsCT
XR_001744857.1:n.1645+19_1645+20delinsCT
XR_001744858.1:n.1645+19_1645+20delinsCT
NM_001354609.2:c.1517+19_1517+20delinsCT	NP_001341538.1:n.1517+19_1517+20delinsCT
NM_001374244.1:c.1637+19_1637+20delinsCT	NP_001361173.1:n.1637+19_1637+20delinsCT
NM_001374258.1:c.1637+19_1637+20delinsCT MANE Plus Clinical	NP_001361187.1:n.1637+19_1637+20delinsCT
NM_004333.6:c.1517+19_1517+20delinsCT MANE Select	NP_004324.2:n.1517+19_1517+20delinsCT
NM_001378467.1:c.1526+19_1526+20delinsCT	NP_001365396.1:n.1526+19_1526+20delinsCT
NM_001378468.1:c.1517+19_1517+20delinsCT	NP_001365397.1:n.1517+19_1517+20delinsCT
NM_001378469.1:c.1451+19_1451+20delinsCT	NP_001365398.1:n.1451+19_1451+20delinsCT
NM_001378470.1:c.1415+19_1415+20delinsCT	NP_001365399.1:n.1415+19_1415+20delinsCT
NM_001378471.1:c.1406+19_1406+20delinsCT	NP_001365400.1:n.1406+19_1406+20delinsCT
NM_001378472.1:c.1361+19_1361+20delinsCT	NP_001365401.1:n.1361+19_1361+20delinsCT
NM_001378473.1:c.1361+19_1361+20delinsCT	NP_001365402.1:n.1361+19_1361+20delinsCT
NM_001378474.1:c.1517+19_1517+20delinsCT	NP_001365403.1:n.1517+19_1517+20delinsCT
NM_001378475.1:c.1253+19_1253+20delinsCT	NP_001365404.1:n.1253+19_1253+20delinsCT