Canonical Allele Identifier: CA454608735
Gene: GCK HGNC NCBI

Linked Data

gnomAD v4: 7-44147775-C-T
MyVariant Identifiers: chr7:g.44187374C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44147775C>T , CM000669.2:g.44147775C>T GRCh38
NC_000007.13:g.44187374C>T , CM000669.1:g.44187374C>T GRCh37
NC_000007.12:g.44153899C>T NCBI36
NG_008847.1:g.46649G>A
NG_008847.2:g.55396G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*736G>A ENSP00000379142.4:n.*736G>A
ENST00000616242.5:c.738G>A ENSP00000482149.2:p.Gly246=
ENST00000345378.7:c.741G>A ENSP00000223366.2:p.Gly247=
ENST00000403799.8:c.738G>A MANE Select ENSP00000384247.3:p.Gly246=
ENST00000671824.1:c.738G>A ENSP00000500264.1:p.Gly246=
ENST00000673284.1:c.738G>A ENSP00000499852.1:p.Gly246=
ENST00000345378.6:c.741G>A ENSP00000223366.2:p.Gly247=
ENST00000395796.7:c.735G>A ENSP00000379142.3:p.Gly245=
ENST00000403799.7:c.738G>A ENSP00000384247.3:p.Gly246=
ENST00000437084.1:c.687G>A ENSP00000402840.1:p.Gly229=
ENST00000616242.4:c.735G>A ENSP00000482149.1:p.Gly245=
NM_000162.3:c.738G>A NP_000153.1:p.Gly246=
NM_033507.1:c.741G>A NP_277042.1:p.Gly247=
NM_033508.1:c.735G>A NP_277043.1:p.Gly245=
XR_927223.1:n.82+27C>T
NM_000162.4:c.738G>A NP_000153.1:p.Gly246=
NM_001354800.1:c.738G>A NP_001341729.1:p.Gly246=
NM_033507.2:c.741G>A NP_277042.1:p.Gly247=
NM_033508.2:c.735G>A NP_277043.1:p.Gly245=
XR_927223.2:n.82+27C>T
NM_000162.5:c.738G>A MANE Select NP_000153.1:p.Gly246=
NM_033507.3:c.741G>A NP_277042.1:p.Gly247=
NM_033508.3:c.735G>A NP_277043.1:p.Gly245=
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