Canonical Allele Identifier: CA2580077574
Gene: BRAF HGNC NCBI

Linked Data

ClinVar Variation Id: 1711067
ClinVar RCV Id: RCV002292354

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140753353_140753354insATA , CM000669.2:g.140753353_140753354insATA GRCh38
NC_000007.13:g.140453153_140453154insATA , CM000669.1:g.140453153_140453154insATA GRCh37
NC_000007.12:g.140099622_140099623insATA NCBI36
NG_007873.3:g.176412_176413insATT , LRG_299:g.176412_176413insATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000646891.2:c.1782_1783insATT MANE Select ENSP00000493543.1:p.Asp594_Phe595insIle
ENST00000288602.11:c.1902_1903insATT ENSP00000288602.7:p.Asp634_Phe635insIle
ENST00000479537.6:c.452_453insATT
ENST00000496384.7:c.1782_1783insATT ENSP00000419060.2:p.Asp594_Phe595insIle
ENST00000497784.2:c.*1232_*1233insATT ENSP00000420119.2:n.*1232_*1233insATT
ENST00000642228.1:c.*860_*861insATT ENSP00000493678.1:n.*860_*861insATT
ENST00000642875.1:n.1259-3935_1259-3934insATT
ENST00000644120.1:n.2172_2173insATT
ENST00000644650.1:c.878_879insATT
ENST00000644905.1:n.2664_2665insATT
ENST00000644969.2:c.1902_1903insATT MANE Plus Clinical ENSP00000496776.1:p.Asp634_Phe635insIle
ENST00000646730.1:c.*358_*359insATT ENSP00000494784.1:n.*358_*359insATT
ENST00000646891.1:c.1782_1783insATT ENSP00000493543.1:p.Asp594_Phe595insIle
ENST00000647434.1:c.738-3935_738-3934insATT ENSP00000495132.1:n.738-3935_738-3934insATT
ENST00000288602.10:c.1782_1783insATT ENSP00000288602.6:p.Asp594_Phe595insIle
ENST00000479537.5:c.66_67insATT ENSP00000418033.1:p.Asp22_Phe23insIle
ENST00000496384.6:c.605_606insATT
ENST00000497784.1:c.1817_1818insATT ENSP00000420119.1:n.1817_1818insATT
NM_004333.4:c.1782_1783insATT , LRG_299t1:c.1782_1783insATT NP_004324.2:p.Asp594_Phe595insIle
XM_005250045.1:c.1782_1783insATT XP_005250102.1:p.Asp594_Phe595insIle
XM_005250046.1:c.1782_1783insATT XP_005250103.1:p.Asp594_Phe595insIle
XM_011516529.1:c.1782_1783insATT XP_011514831.1:p.Asp594_Phe595insIle
XM_011516530.1:c.1695-3935_1695-3934insATT XP_011514832.1:n.1695-3935_1695-3934insATT
XR_242190.1:n.1790_1791insATT
XR_927520.1:n.1790_1791insATT
XR_927521.1:n.1790_1791insATT
XR_927522.1:n.1703-3935_1703-3934insATT
XR_927523.1:n.1703-3935_1703-3934insATT
NM_001354609.1:c.1782_1783insATT NP_001341538.1:p.Asp594_Phe595insIle
NM_004333.5:c.1782_1783insATT NP_004324.2:p.Asp594_Phe595insIle
NR_148928.1:n.2880_2881insATT
XM_017012558.1:c.1902_1903insATT XP_016868047.1:p.Asp634_Phe635insIle
XM_017012559.1:c.1902_1903insATT XP_016868048.1:p.Asp634_Phe635insIle
XR_001744857.1:n.1910_1911insATT
XR_001744858.1:n.1823-3935_1823-3934insATT
NM_001354609.2:c.1782_1783insATT NP_001341538.1:p.Asp594_Phe595insIle
NM_001374244.1:c.1902_1903insATT NP_001361173.1:p.Asp634_Phe635insIle
NM_001374258.1:c.1902_1903insATT MANE Plus Clinical NP_001361187.1:p.Asp634_Phe635insIle
NM_004333.6:c.1782_1783insATT MANE Select NP_004324.2:p.Asp594_Phe595insIle
NM_001378467.1:c.1791_1792insATT NP_001365396.1:p.Asp597_Phe598insIle
NM_001378468.1:c.1782_1783insATT NP_001365397.1:p.Asp594_Phe595insIle
NM_001378469.1:c.1716_1717insATT NP_001365398.1:p.Asp572_Phe573insIle
NM_001378470.1:c.1680_1681insATT NP_001365399.1:p.Asp560_Phe561insIle
NM_001378471.1:c.1671_1672insATT NP_001365400.1:p.Asp557_Phe558insIle
NM_001378472.1:c.1626_1627insATT NP_001365401.1:p.Asp542_Phe543insIle
NM_001378473.1:c.1626_1627insATT NP_001365402.1:p.Asp542_Phe543insIle
NM_001378474.1:c.1782_1783insATT NP_001365403.1:p.Asp594_Phe595insIle
NM_001378475.1:c.1518_1519insATT NP_001365404.1:p.Asp506_Phe507insIle