Canonical Allele Identifier: CA454863298

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44185239G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44145640G>A , CM000669.2:g.44145640G>A	GRCh38
NC_000007.13:g.44185239G>A , CM000669.1:g.44185239G>A	GRCh37
NC_000007.12:g.44151764G>A	NCBI36
NG_008847.1:g.48784C>T
NG_008847.2:g.57531C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*1108C>T	ENSP00000379142.4:n.*1108C>T
ENST00000616242.5:c.*230C>T	ENSP00000482149.2:n.*230C>T
ENST00000683378.1:n.336C>T
ENST00000336642.9:c.144C>T	ENSP00000338009.5:p.Ala48=
ENST00000345378.7:c.1113C>T	ENSP00000223366.2:p.Ala371=
ENST00000403799.8:c.1110C>T MANE Select	ENSP00000384247.3:p.Ala370=
ENST00000671824.1:c.1173C>T	ENSP00000500264.1:p.Ala391=
ENST00000672743.1:n.122C>T
ENST00000673284.1:c.1110C>T	ENSP00000499852.1:p.Ala370=
ENST00000336642.8:c.162C>T	ENSP00000338009.4:p.Ala54=
ENST00000345378.6:c.1113C>T	ENSP00000223366.2:p.Ala371=
ENST00000395796.7:c.1107C>T	ENSP00000379142.3:p.Ala369=
ENST00000403799.7:c.1110C>T	ENSP00000384247.3:p.Ala370=
ENST00000437084.1:c.1059C>T	ENSP00000402840.1:p.Ala353=
ENST00000459642.1:n.490C>T
ENST00000616242.4:c.1107C>T	ENSP00000482149.1:p.Ala369=
NM_000162.3:c.1110C>T	NP_000153.1:p.Ala370=
NM_033507.1:c.1113C>T	NP_277042.1:p.Ala371=
NM_033508.1:c.1107C>T	NP_277043.1:p.Ala369=
NM_000162.4:c.1110C>T	NP_000153.1:p.Ala370=
NM_001354800.1:c.1110C>T	NP_001341729.1:p.Ala370=
NM_001354801.1:c.99C>T	NP_001341730.1:p.Ala33=
NM_001354802.1:c.-31C>T	NP_001341731.1:n.-31C>T
NM_001354803.1:c.144C>T	NP_001341732.1:p.Ala48=
NM_033507.2:c.1113C>T	NP_277042.1:p.Ala371=
NM_033508.2:c.1107C>T	NP_277043.1:p.Ala369=
XM_024446707.1:c.-31C>T	XP_024302475.1:n.-31C>T
NM_000162.5:c.1110C>T MANE Select	NP_000153.1:p.Ala370=
NM_033507.3:c.1113C>T	NP_277042.1:p.Ala371=
NM_033508.3:c.1107C>T	NP_277043.1:p.Ala369=
NM_001354803.2:c.144C>T	NP_001341732.1:p.Ala48=