Canonical Allele Identifier: CA454607772

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44186094G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44146495G>T , CM000669.2:g.44146495G>T	GRCh38
NC_000007.13:g.44186094G>T , CM000669.1:g.44186094G>T	GRCh37
NC_000007.12:g.44152619G>T	NCBI36
NG_008847.1:g.47929C>A
NG_008847.2:g.56676C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*985C>A	ENSP00000379142.4:n.*985C>A
ENST00000616242.5:c.*107C>A	ENSP00000482149.2:n.*107C>A
ENST00000683378.1:n.213C>A
ENST00000345378.7:c.990C>A	ENSP00000223366.2:p.Ala330=
ENST00000403799.8:c.987C>A MANE Select	ENSP00000384247.3:p.Ala329=
ENST00000671824.1:c.1050C>A	ENSP00000500264.1:p.Ala350=
ENST00000673284.1:c.987C>A	ENSP00000499852.1:p.Ala329=
ENST00000345378.6:c.990C>A	ENSP00000223366.2:p.Ala330=
ENST00000395796.7:c.984C>A	ENSP00000379142.3:p.Ala328=
ENST00000403799.7:c.987C>A	ENSP00000384247.3:p.Ala329=
ENST00000437084.1:c.936C>A	ENSP00000402840.1:p.Ala312=
ENST00000473353.1:n.285C>A
ENST00000616242.4:c.984C>A	ENSP00000482149.1:p.Ala328=
NM_000162.3:c.987C>A	NP_000153.1:p.Ala329=
NM_033507.1:c.990C>A	NP_277042.1:p.Ala330=
NM_033508.1:c.984C>A	NP_277043.1:p.Ala328=
NM_000162.4:c.987C>A	NP_000153.1:p.Ala329=
NM_001354800.1:c.987C>A	NP_001341729.1:p.Ala329=
NM_001354801.1:c.8+124C>A	NP_001341730.1:n.8+124C>A
NM_033507.2:c.990C>A	NP_277042.1:p.Ala330=
NM_033508.2:c.984C>A	NP_277043.1:p.Ala328=
NM_000162.5:c.987C>A MANE Select	NP_000153.1:p.Ala329=
NM_033507.3:c.990C>A	NP_277042.1:p.Ala330=
NM_033508.3:c.984C>A	NP_277043.1:p.Ala328=