Canonical Allele Identifier: CA454863166

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44185155G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145556G>A , CM000669.2:g.44145556G>A	GRCh38
NC_000007.13:g.44185155G>A , CM000669.1:g.44185155G>A	GRCh37
NC_000007.12:g.44151680G>A	NCBI36
NG_008847.1:g.48868C>T
NG_008847.2:g.57615C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1192C>T	ENSP00000379142.4:n.*1192C>T
ENST00000616242.5:c.*314C>T	ENSP00000482149.2:n.*314C>T
ENST00000683378.1:n.420C>T
ENST00000336642.9:c.228C>T	ENSP00000338009.5:p.Ser76=
ENST00000345378.7:c.1197C>T	ENSP00000223366.2:p.Ser399=
ENST00000403799.8:c.1194C>T MANE Select	ENSP00000384247.3:p.Ser398=
ENST00000671824.1:c.1257C>T	ENSP00000500264.1:p.Ser419=
ENST00000672743.1:n.206C>T
ENST00000673284.1:c.1194C>T	ENSP00000499852.1:p.Ser398=
ENST00000336642.8:c.246C>T	ENSP00000338009.4:p.Ser82=
ENST00000345378.6:c.1197C>T	ENSP00000223366.2:p.Ser399=
ENST00000395796.7:c.1191C>T	ENSP00000379142.3:p.Ser397=
ENST00000403799.7:c.1194C>T	ENSP00000384247.3:p.Ser398=
ENST00000437084.1:c.1143C>T	ENSP00000402840.1:p.Ser381=
ENST00000459642.1:n.574C>T
ENST00000616242.4:c.1191C>T	ENSP00000482149.1:p.Ser397=
NM_000162.3:c.1194C>T	NP_000153.1:p.Ser398=
NM_033507.1:c.1197C>T	NP_277042.1:p.Ser399=
NM_033508.1:c.1191C>T	NP_277043.1:p.Ser397=
NM_000162.4:c.1194C>T	NP_000153.1:p.Ser398=
NM_001354800.1:c.1194C>T	NP_001341729.1:p.Ser398=
NM_001354801.1:c.183C>T	NP_001341730.1:p.Ser61=
NM_001354802.1:c.54C>T	NP_001341731.1:p.Ser18=
NM_001354803.1:c.228C>T	NP_001341732.1:p.Ser76=
NM_033507.2:c.1197C>T	NP_277042.1:p.Ser399=
NM_033508.2:c.1191C>T	NP_277043.1:p.Ser397=
XM_024446707.1:c.54C>T	XP_024302475.1:p.Ser18=
NM_000162.5:c.1194C>T MANE Select	NP_000153.1:p.Ser398=
NM_033507.3:c.1197C>T	NP_277042.1:p.Ser399=
NM_033508.3:c.1191C>T	NP_277043.1:p.Ser397=
NM_001354803.2:c.228C>T	NP_001341732.1:p.Ser76=