Canonical Allele Identifier: CA8056830

Gene: AKTIP

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.53492507G>C , CM000678.2:g.53492507G>C	GRCh38
NC_000016.9:g.53526419G>C , CM000678.1:g.53526419G>C	GRCh37
NC_000016.8:g.52083920G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394657.12:c.784C>G MANE Select	ENSP00000378152.6:p.Gln262Glu
ENST00000300245.8:c.787C>G	ENSP00000300245.4:p.Gln263Glu
ENST00000394657.11:c.784C>G	ENSP00000378152.6:p.Gln262Glu
ENST00000565431.1:n.255C>G
ENST00000570004.5:c.784C>G	ENSP00000455874.1:p.Gln262Glu
ENST00000571523.2:n.1462C>G
NM_001012398.1:c.784C>G	NP_001012398.1:p.Gln262Glu
NM_001012398.2:c.784C>G	NP_001012398.1:p.Gln262Glu
NM_001308325.1:c.787C>G	NP_001295254.1:p.Gln263Glu
NM_022476.2:c.784C>G	NP_071921.1:p.Gln262Glu
NM_022476.3:c.784C>G	NP_071921.1:p.Gln262Glu
XM_005256095.3:c.787C>G	XP_005256152.1:p.Gln263Glu
XM_005256096.3:c.787C>G	XP_005256153.1:p.Gln263Glu
XM_005256097.3:c.787C>G	XP_005256154.1:p.Gln263Glu
XM_005256098.3:c.787C>G	XP_005256155.1:p.Gln263Glu
XM_005256095.5:c.787C>G	XP_005256152.1:p.Gln263Glu
XM_005256096.5:c.787C>G	XP_005256153.1:p.Gln263Glu
XM_005256097.5:c.787C>G	XP_005256154.1:p.Gln263Glu
XM_005256098.5:c.787C>G	XP_005256155.1:p.Gln263Glu
XM_017023564.2:c.784C>G	XP_016879053.1:p.Gln262Glu
XM_017023565.1:c.784C>G	XP_016879054.1:p.Gln262Glu
XM_017023566.1:c.784C>G	XP_016879055.1:p.Gln262Glu
NM_022476.4:c.784C>G MANE Select	NP_071921.1:p.Gln262Glu
NM_001012398.3:c.784C>G	NP_001012398.1:p.Gln262Glu
NM_001308325.2:c.787C>G	NP_001295254.1:p.Gln263Glu