Canonical Allele Identifier: CA15078881

Gene: UCK2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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