Canonical Allele Identifier: CA454863151

Gene: GCK

Linked Data

• gnomAD v4: 7-44145541-G-T
• MyVariant Identifiers: chr7:g.44185140G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145541G>T , CM000669.2:g.44145541G>T	GRCh38
NC_000007.13:g.44185140G>T , CM000669.1:g.44185140G>T	GRCh37
NC_000007.12:g.44151665G>T	NCBI36
NG_008847.1:g.48883C>A
NG_008847.2:g.57630C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1207C>A	ENSP00000379142.4:n.*1207C>A
ENST00000616242.5:c.*329C>A	ENSP00000482149.2:n.*329C>A
ENST00000683378.1:n.435C>A
ENST00000336642.9:c.243C>A	ENSP00000338009.5:p.Arg81=
ENST00000345378.7:c.1212C>A	ENSP00000223366.2:p.Arg404=
ENST00000403799.8:c.1209C>A MANE Select	ENSP00000384247.3:p.Arg403=
ENST00000671824.1:c.1272C>A	ENSP00000500264.1:p.Arg424=
ENST00000672743.1:n.221C>A
ENST00000673284.1:c.1209C>A	ENSP00000499852.1:p.Arg403=
ENST00000336642.8:c.261C>A	ENSP00000338009.4:p.Arg87=
ENST00000345378.6:c.1212C>A	ENSP00000223366.2:p.Arg404=
ENST00000395796.7:c.1206C>A	ENSP00000379142.3:p.Arg402=
ENST00000403799.7:c.1209C>A	ENSP00000384247.3:p.Arg403=
ENST00000437084.1:c.1158C>A	ENSP00000402840.1:p.Arg386=
ENST00000459642.1:n.589C>A
ENST00000616242.4:c.1206C>A	ENSP00000482149.1:p.Arg402=
NM_000162.3:c.1209C>A	NP_000153.1:p.Arg403=
NM_033507.1:c.1212C>A	NP_277042.1:p.Arg404=
NM_033508.1:c.1206C>A	NP_277043.1:p.Arg402=
NM_000162.4:c.1209C>A	NP_000153.1:p.Arg403=
NM_001354800.1:c.1209C>A	NP_001341729.1:p.Arg403=
NM_001354801.1:c.198C>A	NP_001341730.1:p.Arg66=
NM_001354802.1:c.69C>A	NP_001341731.1:p.Arg23=
NM_001354803.1:c.243C>A	NP_001341732.1:p.Arg81=
NM_033507.2:c.1212C>A	NP_277042.1:p.Arg404=
NM_033508.2:c.1206C>A	NP_277043.1:p.Arg402=
XM_024446707.1:c.69C>A	XP_024302475.1:p.Arg23=
NM_000162.5:c.1209C>A MANE Select	NP_000153.1:p.Arg403=
NM_033507.3:c.1212C>A	NP_277042.1:p.Arg404=
NM_033508.3:c.1206C>A	NP_277043.1:p.Arg402=
NM_001354803.2:c.243C>A	NP_001341732.1:p.Arg81=