Canonical Allele Identifier: CA4239485

Gene: GCK

Linked Data

• dbSNP Id: rs748431922
• ExAC: 7:44186199 A / G
• gnomAD v4: 7-44146600-A-G
• MyVariant Identifiers: chr7:g.44186199A>G (hg19) ; chr7:g.44146600A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44146600A>G , CM000669.2:g.44146600A>G	GRCh38
NC_000007.13:g.44186199A>G , CM000669.1:g.44186199A>G	GRCh37
NC_000007.12:g.44152724A>G	NCBI36
NG_008847.1:g.47824T>C
NG_008847.2:g.56571T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*880T>C	ENSP00000379142.4:n.*880T>C
ENST00000616242.5:c.*2T>C	ENSP00000482149.2:n.*2T>C
ENST00000683378.1:n.108T>C
ENST00000345378.7:c.885T>C	ENSP00000223366.2:p.Gly295=
ENST00000403799.8:c.882T>C MANE Select	ENSP00000384247.3:p.Gly294=
ENST00000671824.1:c.945T>C	ENSP00000500264.1:p.Gly315=
ENST00000673284.1:c.882T>C	ENSP00000499852.1:p.Gly294=
ENST00000345378.6:c.885T>C	ENSP00000223366.2:p.Gly295=
ENST00000395796.7:c.879T>C	ENSP00000379142.3:p.Gly293=
ENST00000403799.7:c.882T>C	ENSP00000384247.3:p.Gly294=
ENST00000437084.1:c.831T>C	ENSP00000402840.1:p.Gly277=
ENST00000473353.1:n.180T>C
ENST00000616242.4:c.879T>C	ENSP00000482149.1:p.Gly293=
NM_000162.3:c.882T>C	NP_000153.1:p.Gly294=
NM_033507.1:c.885T>C	NP_277042.1:p.Gly295=
NM_033508.1:c.879T>C	NP_277043.1:p.Gly293=
NM_000162.4:c.882T>C	NP_000153.1:p.Gly294=
NM_001354800.1:c.882T>C	NP_001341729.1:p.Gly294=
NM_001354801.1:c.8+19T>C	NP_001341730.1:n.8+19T>C
NM_033507.2:c.885T>C	NP_277042.1:p.Gly295=
NM_033508.2:c.879T>C	NP_277043.1:p.Gly293=
NM_000162.5:c.882T>C MANE Select	NP_000153.1:p.Gly294=
NM_033507.3:c.885T>C	NP_277042.1:p.Gly295=
NM_033508.3:c.879T>C	NP_277043.1:p.Gly293=