Canonical Allele Identifier: CA1581526

Gene: GCKR

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.27498323G>A , CM000664.2:g.27498323G>A	GRCh38
NC_000002.11:g.27721190G>A , CM000664.1:g.27721190G>A	GRCh37
NC_000002.10:g.27574694G>A	NCBI36
NG_028024.1:g.6485G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264717.7:c.354G>A MANE Select	ENSP00000264717.2:p.Ser118=
ENST00000264717.6:c.354G>A	ENSP00000264717.2:p.Ser118=
ENST00000417872.5:c.354G>A	ENSP00000398303.1:p.Ser118=
ENST00000453813.1:c.270G>A	ENSP00000399463.1:p.Ser90=
ENST00000472290.1:n.376G>A
NM_001486.3:c.354G>A	NP_001477.2:p.Ser118=
XM_011532761.1:c.354G>A	XP_011531063.1:p.Ser118=
XM_011532762.1:c.-150G>A	XP_011531064.1:n.-150G>A
XM_011532763.1:c.354G>A	XP_011531065.1:p.Ser118=
XR_001738699.1:n.420G>A
NM_001486.4:c.354G>A MANE Select	NP_001477.2:p.Ser118=