Canonical Allele Identifier: CA3259179728
Community Standard Title: NM_004333.6(BRAF):c.1756_1758delinsAAG (p.Glu586Lys)
Gene: BRAF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.140753377_140753379delinsCTT , CM000669.2:g.140753377_140753379delinsCTT GRCh38
NC_000007.13:g.140453177_140453179delinsCTT , CM000669.1:g.140453177_140453179delinsCTT GRCh37
NC_000007.12:g.140099646_140099648delinsCTT NCBI36
NG_007873.3:g.176386_176388delinsAAG , LRG_299:g.176386_176388delinsAAG

Transcript Alleles

HGVS Amino-acid Change
NM_004333.6:c.1756_1758delinsAAG MANE Select NP_004324.2:p.Glu586Lys
ENST00000646891.2:c.1756_1758delinsAAG MANE Select ENSP00000493543.1:p.Glu586Lys
NM_001374258.1:c.1876_1878delinsAAG MANE Plus Clinical NP_001361187.1:p.Glu626Lys
ENST00000644969.2:c.1876_1878delinsAAG MANE Plus Clinical ENSP00000496776.1:p.Glu626Lys
NM_001354609.1:c.1756_1758delinsAAG NP_001341538.1:p.Glu586Lys
NM_001354609.2:c.1756_1758delinsAAG NP_001341538.1:p.Glu586Lys
NM_001374244.1:c.1876_1878delinsAAG NP_001361173.1:p.Glu626Lys
NM_001378467.1:c.1765_1767delinsAAG NP_001365396.1:p.Glu589Lys
NM_001378468.1:c.1756_1758delinsAAG NP_001365397.1:p.Glu586Lys
NM_001378469.1:c.1690_1692delinsAAG NP_001365398.1:p.Glu564Lys
NM_001378470.1:c.1654_1656delinsAAG NP_001365399.1:p.Glu552Lys
NM_001378471.1:c.1645_1647delinsAAG NP_001365400.1:p.Glu549Lys
NM_001378472.1:c.1600_1602delinsAAG NP_001365401.1:p.Glu534Lys
NM_001378473.1:c.1600_1602delinsAAG NP_001365402.1:p.Glu534Lys
NM_001378474.1:c.1756_1758delinsAAG NP_001365403.1:p.Glu586Lys
NM_001378475.1:c.1492_1494delinsAAG NP_001365404.1:p.Glu498Lys
NM_004333.4:c.1756_1758delinsAAG , LRG_299t1:c.1756_1758delinsAAG NP_004324.2:p.Glu586Lys
NM_004333.5:c.1756_1758delinsAAG NP_004324.2:p.Glu586Lys
NR_148928.1:n.2854_2856delinsAAG
ENST00000288602.10:c.1756_1758delinsAAG ENSP00000288602.6:p.Glu586Lys
ENST00000288602.11:c.1876_1878delinsAAG ENSP00000288602.7:p.Glu626Lys
ENST00000479537.5:c.40_42delinsAAG ENSP00000418033.1:p.Glu14Lys
ENST00000479537.6:c.426_428delinsAAG
ENST00000496384.6:c.579_581delinsAAG
ENST00000496384.7:c.1756_1758delinsAAG ENSP00000419060.2:p.Glu586Lys
ENST00000497784.1:c.1791_1793delinsAAG ENSP00000420119.1:n.1791_1793delinsAAG
ENST00000497784.2:c.*1206_*1208delinsAAG ENSP00000420119.2:n.*1206_*1208delinsAAG
ENST00000642228.1:c.*834_*836delinsAAG ENSP00000493678.1:n.*834_*836delinsAAG
ENST00000642875.1:n.1259-3961_1259-3959delinsAAG
ENST00000644120.1:n.2146_2148delinsAAG
ENST00000644650.1:c.852_854delinsAAG
ENST00000644905.1:n.2638_2640delinsAAG
ENST00000646730.1:c.*332_*334delinsAAG ENSP00000494784.1:n.*332_*334delinsAAG
ENST00000646891.1:c.1756_1758delinsAAG ENSP00000493543.1:p.Glu586Lys
ENST00000647434.1:c.738-3961_738-3959delinsAAG ENSP00000495132.1:n.738-3961_738-3959delinsAAG
XM_005250045.1:c.1756_1758delinsAAG XP_005250102.1:p.Glu586Lys
XM_005250046.1:c.1756_1758delinsAAG XP_005250103.1:p.Glu586Lys
XM_011516529.1:c.1756_1758delinsAAG XP_011514831.1:p.Glu586Lys
XM_011516530.1:c.1695-3961_1695-3959delinsAAG XP_011514832.1:n.1695-3961_1695-3959delinsAAG
XM_017012558.1:c.1876_1878delinsAAG XP_016868047.1:p.Glu626Lys
XM_017012559.1:c.1876_1878delinsAAG XP_016868048.1:p.Glu626Lys
XR_001744857.1:n.1884_1886delinsAAG
XR_001744858.1:n.1823-3961_1823-3959delinsAAG
XR_242190.1:n.1764_1766delinsAAG
XR_927520.1:n.1764_1766delinsAAG
XR_927521.1:n.1764_1766delinsAAG
XR_927522.1:n.1703-3961_1703-3959delinsAAG
XR_927523.1:n.1703-3961_1703-3959delinsAAG