Canonical Allele Identifier: CA1433027131

Gene: GAK

Linked Data

• dbSNP Id: rs1725835557

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.931698_931720del , CM000666.2:g.931698_931720del	GRCh38
NC_000004.11:g.925486_925508del , CM000666.1:g.925486_925508del	GRCh37
NC_000004.10:g.915486_915508del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000314167.9:c.145+332_145+354del MANE Select	ENSP00000314499.4:n.145+332_145+354del
ENST00000314167.8:c.145+332_145+354del	ENSP00000314499.4:n.145+332_145+354del
ENST00000502656.5:c.145+332_145+354del	ENSP00000424701.1:n.145+332_145+354del
ENST00000505819.5:c.145+332_145+354del	ENSP00000426908.1:n.145+332_145+354del
ENST00000507580.5:c.145+332_145+354del	ENSP00000426728.1:n.145+332_145+354del
ENST00000511163.5:c.145+332_145+354del	ENSP00000421361.1:n.145+332_145+354del
ENST00000512325.3:c.145+332_145+354del	ENSP00000421814.1:n.145+332_145+354del
ENST00000513935.1:n.178+332_178+354del
ENST00000618573.4:c.117+360_117+382del	ENSP00000484475.1:n.117+360_117+382del
ENST00000628912.1:c.145+332_145+354del	ENSP00000486984.1:n.145+332_145+354del
NM_001286833.1:c.145+332_145+354del	NP_001273762.1:n.145+332_145+354del
NM_005255.2:c.145+332_145+354del	NP_005246.2:n.145+332_145+354del
XM_005272268.1:c.145+332_145+354del	XP_005272325.1:n.145+332_145+354del
XM_005272270.1:c.145+332_145+354del	XP_005272327.1:n.145+332_145+354del
XM_011513425.1:c.145+332_145+354del	XP_011511727.1:n.145+332_145+354del
XM_011513426.1:c.145+332_145+354del	XP_011511728.1:n.145+332_145+354del
XM_011513427.1:c.145+332_145+354del	XP_011511729.1:n.145+332_145+354del
XM_011513428.1:c.145+332_145+354del	XP_011511730.1:n.145+332_145+354del
XM_011513430.1:c.145+332_145+354del	XP_011511732.1:n.145+332_145+354del
XM_011513431.1:c.145+332_145+354del	XP_011511733.1:n.145+332_145+354del
XM_011513433.1:c.145+332_145+354del	XP_011511735.1:n.145+332_145+354del
XM_011513434.1:c.-89+332_-89+354del	XP_011511736.1:n.-89+332_-89+354del
NM_001318134.1:c.145+332_145+354del	NP_001305063.1:n.145+332_145+354del
NM_005255.3:c.145+332_145+354del	NP_005246.2:n.145+332_145+354del
XM_005272268.2:c.145+332_145+354del	XP_005272325.1:n.145+332_145+354del
XM_005272270.2:c.145+332_145+354del	XP_005272327.1:n.145+332_145+354del
XM_011513425.2:c.145+332_145+354del	XP_011511727.1:n.145+332_145+354del
XM_011513426.2:c.145+332_145+354del	XP_011511728.1:n.145+332_145+354del
XM_011513427.2:c.145+332_145+354del	XP_011511729.1:n.145+332_145+354del
XM_011513428.2:c.145+332_145+354del	XP_011511730.1:n.145+332_145+354del
XM_011513431.2:c.145+332_145+354del	XP_011511733.1:n.145+332_145+354del
XM_011513434.2:c.-89+332_-89+354del	XP_011511736.1:n.-89+332_-89+354del
XM_017007991.1:c.145+332_145+354del	XP_016863480.1:n.145+332_145+354del
XM_017007992.1:c.145+332_145+354del	XP_016863481.1:n.145+332_145+354del
XM_017007994.1:c.145+332_145+354del	XP_016863483.1:n.145+332_145+354del
XM_017007995.1:c.-385+332_-385+354del	XP_016863484.1:n.-385+332_-385+354del
NM_005255.4:c.145+332_145+354del MANE Select	NP_005246.2:n.145+332_145+354del
NM_001318134.2:c.145+332_145+354del	NP_001305063.1:n.145+332_145+354del