Canonical Allele Identifier: CA913112072

Gene: BRAF

Linked Data

• MyVariant Identifiers: chr7:g.140477859_140477860delinsCA (hg19)
• CIViC: CA913112072

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.140778059_140778060delinsCA , CM000669.2:g.140778059_140778060delinsCA	GRCh38
NC_000007.13:g.140477859_140477860delinsCA , CM000669.1:g.140477859_140477860delinsCA	GRCh37
NC_000007.12:g.140124328_140124329delinsCA	NCBI36
NG_007873.3:g.151705_151706delinsTG , LRG_299:g.151705_151706delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000646891.2:c.1448_1449delinsTG MANE Select	ENSP00000493543.1:p.Lys483Met
ENST00000288602.11:c.1568_1569delinsTG	ENSP00000288602.7:p.Lys523Met
ENST00000479537.6:c.118_119delinsTG
ENST00000496384.7:c.1448_1449delinsTG	ENSP00000419060.2:p.Lys483Met
ENST00000497784.2:c.*898_*899delinsTG	ENSP00000420119.2:n.*898_*899delinsTG
ENST00000642228.1:c.*526_*527delinsTG	ENSP00000493678.1:n.*526_*527delinsTG
ENST00000642875.1:n.1012_1013delinsTG
ENST00000644120.1:n.1838_1839delinsTG
ENST00000644650.1:c.544_545delinsTG
ENST00000644905.1:n.1537_1538delinsTG
ENST00000644969.2:c.1568_1569delinsTG MANE Plus Clinical	ENSP00000496776.1:p.Lys523Met
ENST00000646730.1:c.1448_1449delinsTG	ENSP00000494784.1:p.Lys483Met
ENST00000646891.1:c.1448_1449delinsTG	ENSP00000493543.1:p.Lys483Met
ENST00000647434.1:c.491_492delinsTG	ENSP00000495132.1:p.Lys164Met
ENST00000288602.10:c.1448_1449delinsTG	ENSP00000288602.6:p.Lys483Met
ENST00000496384.6:c.271_272delinsTG
ENST00000497784.1:c.1483_1484delinsTG	ENSP00000420119.1:n.1483_1484delinsTG
NM_004333.4:c.1448_1449delinsTG , LRG_299t1:c.1448_1449delinsTG	NP_004324.2:p.Lys483Met
XM_005250045.1:c.1448_1449delinsTG	XP_005250102.1:p.Lys483Met
XM_005250046.1:c.1448_1449delinsTG	XP_005250103.1:p.Lys483Met
XM_011516529.1:c.1448_1449delinsTG	XP_011514831.1:p.Lys483Met
XM_011516530.1:c.1448_1449delinsTG	XP_011514832.1:p.Lys483Met
XR_242190.1:n.1456_1457delinsTG
XR_927520.1:n.1456_1457delinsTG
XR_927521.1:n.1456_1457delinsTG
XR_927522.1:n.1456_1457delinsTG
XR_927523.1:n.1456_1457delinsTG
NM_001354609.1:c.1448_1449delinsTG	NP_001341538.1:p.Lys483Met
NM_004333.5:c.1448_1449delinsTG	NP_004324.2:p.Lys483Met
NR_148928.1:n.1753_1754delinsTG
XM_017012558.1:c.1568_1569delinsTG	XP_016868047.1:p.Lys523Met
XM_017012559.1:c.1568_1569delinsTG	XP_016868048.1:p.Lys523Met
XR_001744857.1:n.1576_1577delinsTG
XR_001744858.1:n.1576_1577delinsTG
NM_001354609.2:c.1448_1449delinsTG	NP_001341538.1:p.Lys483Met
NM_001374244.1:c.1568_1569delinsTG	NP_001361173.1:p.Lys523Met
NM_001374258.1:c.1568_1569delinsTG MANE Plus Clinical	NP_001361187.1:p.Lys523Met
NM_004333.6:c.1448_1449delinsTG MANE Select	NP_004324.2:p.Lys483Met
NM_001378467.1:c.1457_1458delinsTG	NP_001365396.1:p.Lys486Met
NM_001378468.1:c.1448_1449delinsTG	NP_001365397.1:p.Lys483Met
NM_001378469.1:c.1382_1383delinsTG	NP_001365398.1:p.Lys461Met
NM_001378470.1:c.1346_1347delinsTG	NP_001365399.1:p.Lys449Met
NM_001378471.1:c.1337_1338delinsTG	NP_001365400.1:p.Lys446Met
NM_001378472.1:c.1292_1293delinsTG	NP_001365401.1:p.Lys431Met
NM_001378473.1:c.1292_1293delinsTG	NP_001365402.1:p.Lys431Met
NM_001378474.1:c.1448_1449delinsTG	NP_001365403.1:p.Lys483Met
NM_001378475.1:c.1184_1185delinsTG	NP_001365404.1:p.Lys395Met