Canonical Allele Identifier: CA2519067329
Gene: GAK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.931432_931433insCCCCCCCCCCCCCCACC , CM000666.2:g.931432_931433insCCCCCCCCCCCCCCACC GRCh38
NC_000004.11:g.925220_925221insCCCCCCCCCCCCCCACC , CM000666.1:g.925220_925221insCCCCCCCCCCCCCCACC GRCh37
NC_000004.10:g.915220_915221insCCCCCCCCCCCCCCACC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000314167.9:c.145+612_145+613insTGGGGGGGGGGGGGGGG MANE Select ENSP00000314499.4:n.145+612_145+613insTGGGGGGGGGGGGGGGG
ENST00000314167.8:c.145+612_145+613insTGGGGGGGGGGGGGGGG ENSP00000314499.4:n.145+612_145+613insTGGGGGGGGGGGGGGGG
ENST00000502656.5:c.145+612_145+613insTGGGGGGGGGGGGGGGG ENSP00000424701.1:n.145+612_145+613insTGGGGGGGGGGGGGGGG
ENST00000505819.5:c.145+612_145+613insTGGGGGGGGGGGGGGGG ENSP00000426908.1:n.145+612_145+613insTGGGGGGGGGGGGGGGG
ENST00000507580.5:c.145+612_145+613insTGGGGGGGGGGGGGGGG ENSP00000426728.1:n.145+612_145+613insTGGGGGGGGGGGGGGGG
ENST00000511163.5:c.145+612_145+613insTGGGGGGGGGGGGGGGG ENSP00000421361.1:n.145+612_145+613insTGGGGGGGGGGGGGGGG
ENST00000512325.3:c.145+612_145+613insTGGGGGGGGGGGGGGGG ENSP00000421814.1:n.145+612_145+613insTGGGGGGGGGGGGGGGG
ENST00000513935.1:n.178+612_178+613insTGGGGGGGGGGGGGGGG
ENST00000618573.4:c.117+640_117+641insTGGGGGGGGGGGGGGGG ENSP00000484475.1:n.117+640_117+641insTGGGGGGGGGGGGGGGG
ENST00000628912.1:c.145+612_145+613insTGGGGGGGGGGGGGGGG ENSP00000486984.1:n.145+612_145+613insTGGGGGGGGGGGGGGGG
NM_001286833.1:c.145+612_145+613insTGGGGGGGGGGGGGGGG NP_001273762.1:n.145+612_145+613insTGGGGGGGGGGGGGGGG
NM_005255.2:c.145+612_145+613insTGGGGGGGGGGGGGGGG NP_005246.2:n.145+612_145+613insTGGGGGGGGGGGGGGGG
XM_005272268.1:c.145+612_145+613insTGGGGGGGGGGGGGGGG XP_005272325.1:n.145+612_145+613insTGGGGGGGGGGGGGGGG
XM_005272270.1:c.145+612_145+613insTGGGGGGGGGGGGGGGG XP_005272327.1:n.145+612_145+613insTGGGGGGGGGGGGGGGG
XM_011513425.1:c.145+612_145+613insTGGGGGGGGGGGGGGGG XP_011511727.1:n.145+612_145+613insTGGGGGGGGGGGGGGGG
XM_011513426.1:c.145+612_145+613insTGGGGGGGGGGGGGGGG XP_011511728.1:n.145+612_145+613insTGGGGGGGGGGGGGGGG
XM_011513427.1:c.145+612_145+613insTGGGGGGGGGGGGGGGG XP_011511729.1:n.145+612_145+613insTGGGGGGGGGGGGGGGG
XM_011513428.1:c.145+612_145+613insTGGGGGGGGGGGGGGGG XP_011511730.1:n.145+612_145+613insTGGGGGGGGGGGGGGGG
XM_011513430.1:c.145+612_145+613insTGGGGGGGGGGGGGGGG XP_011511732.1:n.145+612_145+613insTGGGGGGGGGGGGGGGG
XM_011513431.1:c.145+612_145+613insTGGGGGGGGGGGGGGGG XP_011511733.1:n.145+612_145+613insTGGGGGGGGGGGGGGGG
XM_011513433.1:c.145+612_145+613insTGGGGGGGGGGGGGGGG XP_011511735.1:n.145+612_145+613insTGGGGGGGGGGGGGGGG
XM_011513434.1:c.-89+612_-89+613insTGGGGGGGGGGGGGGGG XP_011511736.1:n.-89+612_-89+613insTGGGGGGGGGGGGGGGG
NM_001318134.1:c.145+612_145+613insTGGGGGGGGGGGGGGGG NP_001305063.1:n.145+612_145+613insTGGGGGGGGGGGGGGGG
NM_005255.3:c.145+612_145+613insTGGGGGGGGGGGGGGGG NP_005246.2:n.145+612_145+613insTGGGGGGGGGGGGGGGG
XM_005272268.2:c.145+612_145+613insTGGGGGGGGGGGGGGGG XP_005272325.1:n.145+612_145+613insTGGGGGGGGGGGGGGGG
XM_005272270.2:c.145+612_145+613insTGGGGGGGGGGGGGGGG XP_005272327.1:n.145+612_145+613insTGGGGGGGGGGGGGGGG
XM_011513425.2:c.145+612_145+613insTGGGGGGGGGGGGGGGG XP_011511727.1:n.145+612_145+613insTGGGGGGGGGGGGGGGG
XM_011513426.2:c.145+612_145+613insTGGGGGGGGGGGGGGGG XP_011511728.1:n.145+612_145+613insTGGGGGGGGGGGGGGGG
XM_011513427.2:c.145+612_145+613insTGGGGGGGGGGGGGGGG XP_011511729.1:n.145+612_145+613insTGGGGGGGGGGGGGGGG
XM_011513428.2:c.145+612_145+613insTGGGGGGGGGGGGGGGG XP_011511730.1:n.145+612_145+613insTGGGGGGGGGGGGGGGG
XM_011513431.2:c.145+612_145+613insTGGGGGGGGGGGGGGGG XP_011511733.1:n.145+612_145+613insTGGGGGGGGGGGGGGGG
XM_011513434.2:c.-89+612_-89+613insTGGGGGGGGGGGGGGGG XP_011511736.1:n.-89+612_-89+613insTGGGGGGGGGGGGGGGG
XM_017007991.1:c.145+612_145+613insTGGGGGGGGGGGGGGGG XP_016863480.1:n.145+612_145+613insTGGGGGGGGGGGGGGGG
XM_017007992.1:c.145+612_145+613insTGGGGGGGGGGGGGGGG XP_016863481.1:n.145+612_145+613insTGGGGGGGGGGGGGGGG
XM_017007994.1:c.145+612_145+613insTGGGGGGGGGGGGGGGG XP_016863483.1:n.145+612_145+613insTGGGGGGGGGGGGGGGG
XM_017007995.1:c.-385+612_-385+613insTGGGGGGGGGGGGGGGG XP_016863484.1:n.-385+612_-385+613insTGGGGGGGGGGGGGGGG
NM_005255.4:c.145+612_145+613insTGGGGGGGGGGGGGGGG MANE Select NP_005246.2:n.145+612_145+613insTGGGGGGGGGGGGGGGG
NM_001318134.2:c.145+612_145+613insTGGGGGGGGGGGGGGGG NP_001305063.1:n.145+612_145+613insTGGGGGGGGGGGGGGGG