Canonical Allele Identifier: CA367403305

Gene: GCK

Linked Data

• dbSNP Id: rs1583604490
• gnomAD v4: 7-44153331-T-G
• MyVariant Identifiers: chr7:g.44192930T>G (hg19) ; chr7:g.44153331T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44153331T>G , CM000669.2:g.44153331T>G	GRCh38
NC_000007.13:g.44192930T>G , CM000669.1:g.44192930T>G	GRCh37
NC_000007.12:g.44159455T>G	NCBI36
NG_008847.1:g.41093A>C
NG_008847.2:g.49840A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000395796.8:c.*176A>C	ENSP00000379142.4:n.*176A>C
ENST00000616242.5:c.178A>C	ENSP00000482149.2:p.Thr60Pro
ENST00000682635.1:n.664A>C
ENST00000345378.7:c.181A>C	ENSP00000223366.2:p.Thr61Pro
ENST00000403799.8:c.178A>C MANE Select	ENSP00000384247.3:p.Thr60Pro
ENST00000671824.1:c.178A>C	ENSP00000500264.1:p.Thr60Pro
ENST00000673284.1:c.178A>C	ENSP00000499852.1:p.Thr60Pro
ENST00000345378.6:c.181A>C	ENSP00000223366.2:p.Thr61Pro
ENST00000395796.7:c.175A>C	ENSP00000379142.3:p.Thr59Pro
ENST00000403799.7:c.178A>C	ENSP00000384247.3:p.Thr60Pro
ENST00000437084.1:c.178A>C	ENSP00000402840.1:p.Thr60Pro
ENST00000616242.4:c.175A>C	ENSP00000482149.1:p.Thr59Pro
NM_000162.3:c.178A>C	NP_000153.1:p.Thr60Pro
NM_033507.1:c.181A>C	NP_277042.1:p.Thr61Pro
NM_033508.1:c.175A>C	NP_277043.1:p.Thr59Pro
NM_000162.4:c.178A>C	NP_000153.1:p.Thr60Pro
NM_001354800.1:c.178A>C	NP_001341729.1:p.Thr60Pro
NM_033507.2:c.181A>C	NP_277042.1:p.Thr61Pro
NM_033508.2:c.175A>C	NP_277043.1:p.Thr59Pro
NM_000162.5:c.178A>C MANE Select	NP_000153.1:p.Thr60Pro
NM_033507.3:c.181A>C	NP_277042.1:p.Thr61Pro
NM_033508.3:c.175A>C	NP_277043.1:p.Thr59Pro