Canonical Allele Identifier: CA454608100

Gene: GCK

Linked Data

• MyVariant Identifiers: chr7:g.44186184G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.44146585G>C , CM000669.2:g.44146585G>C	GRCh38
NC_000007.13:g.44186184G>C , CM000669.1:g.44186184G>C	GRCh37
NC_000007.12:g.44152709G>C	NCBI36
NG_008847.1:g.47839C>G
NG_008847.2:g.56586C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395796.8:c.*895C>G	ENSP00000379142.4:n.*895C>G
ENST00000616242.5:c.*17C>G	ENSP00000482149.2:n.*17C>G
ENST00000683378.1:n.123C>G
ENST00000345378.7:c.900C>G	ENSP00000223366.2:p.Gly300=
ENST00000403799.8:c.897C>G MANE Select	ENSP00000384247.3:p.Gly299=
ENST00000671824.1:c.960C>G	ENSP00000500264.1:p.Gly320=
ENST00000673284.1:c.897C>G	ENSP00000499852.1:p.Gly299=
ENST00000345378.6:c.900C>G	ENSP00000223366.2:p.Gly300=
ENST00000395796.7:c.894C>G	ENSP00000379142.3:p.Gly298=
ENST00000403799.7:c.897C>G	ENSP00000384247.3:p.Gly299=
ENST00000437084.1:c.846C>G	ENSP00000402840.1:p.Gly282=
ENST00000473353.1:n.195C>G
ENST00000616242.4:c.894C>G	ENSP00000482149.1:p.Gly298=
NM_000162.3:c.897C>G	NP_000153.1:p.Gly299=
NM_033507.1:c.900C>G	NP_277042.1:p.Gly300=
NM_033508.1:c.894C>G	NP_277043.1:p.Gly298=
NM_000162.4:c.897C>G	NP_000153.1:p.Gly299=
NM_001354800.1:c.897C>G	NP_001341729.1:p.Gly299=
NM_001354801.1:c.8+34C>G	NP_001341730.1:n.8+34C>G
NM_033507.2:c.900C>G	NP_277042.1:p.Gly300=
NM_033508.2:c.894C>G	NP_277043.1:p.Gly298=
NM_000162.5:c.897C>G MANE Select	NP_000153.1:p.Gly299=
NM_033507.3:c.900C>G	NP_277042.1:p.Gly300=
NM_033508.3:c.894C>G	NP_277043.1:p.Gly298=