Canonical Allele Identifier: CA454609282

Gene: GCK

Linked Data

• dbSNP Id: rs1085307455
• gnomAD v4: 7-44149977-G-T
• MyVariant Identifiers: chr7:g.44189576G>T (hg19) ; chr7:g.44149977G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44149977G>T , CM000669.2:g.44149977G>T	GRCh38
NC_000007.13:g.44189576G>T , CM000669.1:g.44189576G>T	GRCh37
NC_000007.12:g.44156101G>T	NCBI36
NG_008847.1:g.44447C>A
NG_008847.2:g.53194C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*569C>A	ENSP00000379142.4:n.*569C>A
ENST00000616242.5:c.571C>A	ENSP00000482149.2:p.Arg191=
ENST00000682635.1:n.1057C>A
ENST00000345378.7:c.574C>A	ENSP00000223366.2:p.Arg192=
ENST00000403799.8:c.571C>A MANE Select	ENSP00000384247.3:p.Arg191=
ENST00000671824.1:c.571C>A	ENSP00000500264.1:p.Arg191=
ENST00000673284.1:c.571C>A	ENSP00000499852.1:p.Arg191=
ENST00000345378.6:c.574C>A	ENSP00000223366.2:p.Arg192=
ENST00000395796.7:c.568C>A	ENSP00000379142.3:p.Arg190=
ENST00000403799.7:c.571C>A	ENSP00000384247.3:p.Arg191=
ENST00000437084.1:c.520C>A	ENSP00000402840.1:p.Arg174=
ENST00000616242.4:c.568C>A	ENSP00000482149.1:p.Arg190=
NM_000162.3:c.571C>A	NP_000153.1:p.Arg191=
NM_033507.1:c.574C>A	NP_277042.1:p.Arg192=
NM_033508.1:c.568C>A	NP_277043.1:p.Arg190=
NM_000162.4:c.571C>A	NP_000153.1:p.Arg191=
NM_001354800.1:c.571C>A	NP_001341729.1:p.Arg191=
NM_033507.2:c.574C>A	NP_277042.1:p.Arg192=
NM_033508.2:c.568C>A	NP_277043.1:p.Arg190=
NM_000162.5:c.571C>A MANE Select	NP_000153.1:p.Arg191=
NM_033507.3:c.574C>A	NP_277042.1:p.Arg192=
NM_033508.3:c.568C>A	NP_277043.1:p.Arg190=