Canonical Allele Identifier: CA2580077577
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1711077
ClinVar RCV Id: RCV002292364

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140753365_140753366insTCTAA , CM000669.2:g.140753365_140753366insTCTAA GRCh38
NC_000007.13:g.140453165_140453166insTCTAA , CM000669.1:g.140453165_140453166insTCTAA GRCh37
NC_000007.12:g.140099634_140099635insTCTAA NCBI36
NG_007873.3:g.176399_176400insTTAGA , LRG_299:g.176399_176400insTTAGA

Transcript Alleles

HGVS Amino-acid change
ENST00000646891.2:c.1769_1770insTTAGA MANE Select ENSP00000493543.1:p.Lys591Ter
ENST00000288602.11:c.1889_1890insTTAGA ENSP00000288602.7:p.Lys631Ter
ENST00000479537.6:c.439_440insTTAGA
ENST00000496384.7:c.1769_1770insTTAGA ENSP00000419060.2:p.Lys591Ter
ENST00000497784.2:c.*1219_*1220insTTAGA ENSP00000420119.2:n.*1219_*1220insTTAGA
ENST00000642228.1:c.*847_*848insTTAGA ENSP00000493678.1:n.*847_*848insTTAGA
ENST00000642875.1:n.1259-3948_1259-3947insTTAGA
ENST00000644120.1:n.2159_2160insTTAGA
ENST00000644650.1:c.865_866insTTAGA
ENST00000644905.1:n.2651_2652insTTAGA
ENST00000644969.2:c.1889_1890insTTAGA MANE Plus Clinical ENSP00000496776.1:p.Lys631Ter
ENST00000646730.1:c.*345_*346insTTAGA ENSP00000494784.1:n.*345_*346insTTAGA
ENST00000646891.1:c.1769_1770insTTAGA ENSP00000493543.1:p.Lys591Ter
ENST00000647434.1:c.738-3948_738-3947insTTAGA ENSP00000495132.1:n.738-3948_738-3947insT...
ENST00000288602.10:c.1769_1770insTTAGA ENSP00000288602.6:p.Lys591Ter
ENST00000479537.5:c.53_54insTTAGA ENSP00000418033.1:p.Lys19Ter
ENST00000496384.6:c.592_593insTTAGA
ENST00000497784.1:c.1804_1805insTTAGA ENSP00000420119.1:n.1804_1805insTTAGA
NM_004333.4:c.1769_1770insTTAGA , LRG_299t1:c.1769_1770insTTAGA NP_004324.2:p.Lys591Ter
XM_005250045.1:c.1769_1770insTTAGA XP_005250102.1:p.Lys591Ter
XM_005250046.1:c.1769_1770insTTAGA XP_005250103.1:p.Lys591Ter
XM_011516529.1:c.1769_1770insTTAGA XP_011514831.1:p.Lys591Ter
XM_011516530.1:c.1695-3948_1695-3947insTTAGA XP_011514832.1:n.1695-3948_1695-3947insTT...
XR_242190.1:n.1777_1778insTTAGA
XR_927520.1:n.1777_1778insTTAGA
XR_927521.1:n.1777_1778insTTAGA
XR_927522.1:n.1703-3948_1703-3947insTTAGA
XR_927523.1:n.1703-3948_1703-3947insTTAGA
NM_001354609.1:c.1769_1770insTTAGA NP_001341538.1:p.Lys591Ter
NM_004333.5:c.1769_1770insTTAGA NP_004324.2:p.Lys591Ter
NR_148928.1:n.2867_2868insTTAGA
XM_017012558.1:c.1889_1890insTTAGA XP_016868047.1:p.Lys631Ter
XM_017012559.1:c.1889_1890insTTAGA XP_016868048.1:p.Lys631Ter
XR_001744857.1:n.1897_1898insTTAGA
XR_001744858.1:n.1823-3948_1823-3947insTTAGA
NM_001354609.2:c.1769_1770insTTAGA NP_001341538.1:p.Lys591Ter
NM_001374244.1:c.1889_1890insTTAGA NP_001361173.1:p.Lys631Ter
NM_001374258.1:c.1889_1890insTTAGA MANE Plus Clinical NP_001361187.1:p.Lys631Ter
NM_004333.6:c.1769_1770insTTAGA MANE Select NP_004324.2:p.Lys591Ter
NM_001378467.1:c.1778_1779insTTAGA NP_001365396.1:p.Lys594Ter
NM_001378468.1:c.1769_1770insTTAGA NP_001365397.1:p.Lys591Ter
NM_001378469.1:c.1703_1704insTTAGA NP_001365398.1:p.Lys569Ter
NM_001378470.1:c.1667_1668insTTAGA NP_001365399.1:p.Lys557Ter
NM_001378471.1:c.1658_1659insTTAGA NP_001365400.1:p.Lys554Ter
NM_001378472.1:c.1613_1614insTTAGA NP_001365401.1:p.Lys539Ter
NM_001378473.1:c.1613_1614insTTAGA NP_001365402.1:p.Lys539Ter
NM_001378474.1:c.1769_1770insTTAGA NP_001365403.1:p.Lys591Ter
NM_001378475.1:c.1505_1506insTTAGA NP_001365404.1:p.Lys503Ter