Canonical Allele Identifier: CA1139995884

Gene: UCK2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165904155T= , CM000663.2:g.165904155T=	GRCh38
NC_000001.10:g.165873392T= , CM000663.1:g.165873392T=	GRCh37
NC_000001.9:g.164140016T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367879.9:c.597+876T= MANE Select	ENSP00000356853.4:n.597+876T=
ENST00000475333.2:n.163T=
ENST00000642653.1:c.534+876T=	ENSP00000494961.1:n.534+876T=
ENST00000367879.8:c.597+876T=	ENSP00000356853.4:n.597+876T=
ENST00000462329.5:n.364+876T=
ENST00000463772.5:n.124+876T=
ENST00000464197.5:n.655+876T=
ENST00000469256.6:c.147+876T=	ENSP00000476692.1:n.147+876T=
ENST00000470820.1:c.147+876T=	ENSP00000476327.1:n.147+876T=
ENST00000475333.1:n.90T=
ENST00000479872.5:n.685+876T=
NM_012474.4:c.597+876T=	NP_036606.2:n.597+876T=
XM_011509969.1:c.534+876T=	XP_011508271.1:n.534+876T=
XM_011509970.1:c.378+876T=	XP_011508272.1:n.378+876T=
NM_001363568.1:c.534+876T=	NP_001350497.1:n.534+876T=
XM_011509970.2:c.438+876T=	XP_011508272.2:n.438+876T=
NM_012474.5:c.597+876T= MANE Select	NP_036606.2:n.597+876T=
NM_001363568.2:c.534+876T=	NP_001350497.1:n.534+876T=