Canonical Allele Identifier: CA454606700

Gene: GCK

Linked Data

• gnomAD v4: 7-44145256-G-A
• MyVariant Identifiers: chr7:g.44184855G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145256G>A , CM000669.2:g.44145256G>A	GRCh38
NC_000007.13:g.44184855G>A , CM000669.1:g.44184855G>A	GRCh37
NC_000007.12:g.44151380G>A	NCBI36
NG_008847.1:g.49168C>T
NG_008847.2:g.57915C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1276C>T	ENSP00000379142.4:n.*1276C>T
ENST00000616242.5:c.*398C>T	ENSP00000482149.2:n.*398C>T
ENST00000683378.1:n.504C>T
ENST00000336642.9:c.312C>T	ENSP00000338009.5:p.Ser104=
ENST00000345378.7:c.1281C>T	ENSP00000223366.2:p.Ser427=
ENST00000403799.8:c.1278C>T MANE Select	ENSP00000384247.3:p.Ser426=
ENST00000671824.1:c.1341C>T	ENSP00000500264.1:p.Ser447=
ENST00000672743.1:n.290C>T
ENST00000673284.1:c.1278C>T	ENSP00000499852.1:p.Ser426=
ENST00000336642.8:c.330C>T	ENSP00000338009.4:p.Ser110=
ENST00000345378.6:c.1281C>T	ENSP00000223366.2:p.Ser427=
ENST00000395796.7:c.1275C>T	ENSP00000379142.3:p.Ser425=
ENST00000403799.7:c.1278C>T	ENSP00000384247.3:p.Ser426=
ENST00000437084.1:c.1227C>T	ENSP00000402840.1:p.Ser409=
ENST00000459642.1:n.658C>T
ENST00000616242.4:c.1275C>T	ENSP00000482149.1:p.Ser425=
NM_000162.3:c.1278C>T	NP_000153.1:p.Ser426=
NM_033507.1:c.1281C>T	NP_277042.1:p.Ser427=
NM_033508.1:c.1275C>T	NP_277043.1:p.Ser425=
NM_000162.4:c.1278C>T	NP_000153.1:p.Ser426=
NM_001354800.1:c.1278C>T	NP_001341729.1:p.Ser426=
NM_001354801.1:c.267C>T	NP_001341730.1:p.Ser89=
NM_001354802.1:c.138C>T	NP_001341731.1:p.Ser46=
NM_001354803.1:c.312C>T	NP_001341732.1:p.Ser104=
NM_033507.2:c.1281C>T	NP_277042.1:p.Ser427=
NM_033508.2:c.1275C>T	NP_277043.1:p.Ser425=
XM_024446707.1:c.138C>T	XP_024302475.1:p.Ser46=
NM_000162.5:c.1278C>T MANE Select	NP_000153.1:p.Ser426=
NM_033507.3:c.1281C>T	NP_277042.1:p.Ser427=
NM_033508.3:c.1275C>T	NP_277043.1:p.Ser425=
NM_001354803.2:c.312C>T	NP_001341732.1:p.Ser104=