Canonical Allele Identifier: CA454609083

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44189411C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44149812C>G , CM000669.2:g.44149812C>G	GRCh38
NC_000007.13:g.44189411C>G , CM000669.1:g.44189411C>G	GRCh37
NC_000007.12:g.44155936C>G	NCBI36
NG_008847.1:g.44612G>C
NG_008847.2:g.53359G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*625G>C	ENSP00000379142.4:n.*625G>C
ENST00000616242.5:c.627G>C	ENSP00000482149.2:p.Thr209=
ENST00000682635.1:n.1113G>C
ENST00000345378.7:c.630G>C	ENSP00000223366.2:p.Thr210=
ENST00000403799.8:c.627G>C MANE Select	ENSP00000384247.3:p.Thr209=
ENST00000671824.1:c.627G>C	ENSP00000500264.1:p.Thr209=
ENST00000673284.1:c.627G>C	ENSP00000499852.1:p.Thr209=
ENST00000345378.6:c.630G>C	ENSP00000223366.2:p.Thr210=
ENST00000395796.7:c.624G>C	ENSP00000379142.3:p.Thr208=
ENST00000403799.7:c.627G>C	ENSP00000384247.3:p.Thr209=
ENST00000437084.1:c.576G>C	ENSP00000402840.1:p.Thr192=
ENST00000616242.4:c.624G>C	ENSP00000482149.1:p.Thr208=
NM_000162.3:c.627G>C	NP_000153.1:p.Thr209=
NM_033507.1:c.630G>C	NP_277042.1:p.Thr210=
NM_033508.1:c.624G>C	NP_277043.1:p.Thr208=
NM_000162.4:c.627G>C	NP_000153.1:p.Thr209=
NM_001354800.1:c.627G>C	NP_001341729.1:p.Thr209=
NM_033507.2:c.630G>C	NP_277042.1:p.Thr210=
NM_033508.2:c.624G>C	NP_277043.1:p.Thr208=
NM_000162.5:c.627G>C MANE Select	NP_000153.1:p.Thr209=
NM_033507.3:c.630G>C	NP_277042.1:p.Thr210=
NM_033508.3:c.624G>C	NP_277043.1:p.Thr208=