Canonical Allele Identifier: CA454608707

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44187335G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44147736G>T , CM000669.2:g.44147736G>T	GRCh38
NC_000007.13:g.44187335G>T , CM000669.1:g.44187335G>T	GRCh37
NC_000007.12:g.44153860G>T	NCBI36
NG_008847.1:g.46688C>A
NG_008847.2:g.55435C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*775C>A	ENSP00000379142.4:n.*775C>A
ENST00000616242.5:c.777C>A	ENSP00000482149.2:p.Ala259=
ENST00000345378.7:c.780C>A	ENSP00000223366.2:p.Ala260=
ENST00000403799.8:c.777C>A MANE Select	ENSP00000384247.3:p.Ala259=
ENST00000671824.1:c.777C>A	ENSP00000500264.1:p.Ala259=
ENST00000673284.1:c.777C>A	ENSP00000499852.1:p.Ala259=
ENST00000345378.6:c.780C>A	ENSP00000223366.2:p.Ala260=
ENST00000395796.7:c.774C>A	ENSP00000379142.3:p.Ala258=
ENST00000403799.7:c.777C>A	ENSP00000384247.3:p.Ala259=
ENST00000437084.1:c.726C>A	ENSP00000402840.1:p.Ala242=
ENST00000616242.4:c.774C>A	ENSP00000482149.1:p.Ala258=
NM_000162.3:c.777C>A	NP_000153.1:p.Ala259=
NM_033507.1:c.780C>A	NP_277042.1:p.Ala260=
NM_033508.1:c.774C>A	NP_277043.1:p.Ala258=
XR_927223.1:n.70G>T
NM_000162.4:c.777C>A	NP_000153.1:p.Ala259=
NM_001354800.1:c.777C>A	NP_001341729.1:p.Ala259=
NM_033507.2:c.780C>A	NP_277042.1:p.Ala260=
NM_033508.2:c.774C>A	NP_277043.1:p.Ala258=
XR_927223.2:n.70G>T
NM_000162.5:c.777C>A MANE Select	NP_000153.1:p.Ala259=
NM_033507.3:c.780C>A	NP_277042.1:p.Ala260=
NM_033508.3:c.774C>A	NP_277043.1:p.Ala258=