Canonical Allele Identifier: CA454610668
Gene: GCK HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.44193035G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44153436G>A , CM000669.2:g.44153436G>A GRCh38
NC_000007.13:g.44193035G>A , CM000669.1:g.44193035G>A GRCh37
NC_000007.12:g.44159560G>A NCBI36
NG_008847.1:g.40988C>T
NG_008847.2:g.49735C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*71C>T ENSP00000379142.4:n.*71C>T
ENST00000616242.5:c.73C>T ENSP00000482149.2:p.Leu25=
ENST00000682635.1:n.559C>T
ENST00000345378.7:c.76C>T ENSP00000223366.2:p.Leu26=
ENST00000403799.8:c.73C>T MANE Select ENSP00000384247.3:p.Leu25=
ENST00000671824.1:c.73C>T ENSP00000500264.1:p.Leu25=
ENST00000673284.1:c.73C>T ENSP00000499852.1:p.Leu25=
ENST00000345378.6:c.76C>T ENSP00000223366.2:p.Leu26=
ENST00000395796.7:c.70C>T ENSP00000379142.3:p.Leu24=
ENST00000403799.7:c.73C>T ENSP00000384247.3:p.Leu25=
ENST00000437084.1:c.73C>T ENSP00000402840.1:p.Leu25=
ENST00000476008.1:n.508C>T
ENST00000616242.4:c.70C>T ENSP00000482149.1:p.Leu24=
NM_000162.3:c.73C>T NP_000153.1:p.Leu25=
NM_033507.1:c.76C>T NP_277042.1:p.Leu26=
NM_033508.1:c.70C>T NP_277043.1:p.Leu24=
NM_000162.4:c.73C>T NP_000153.1:p.Leu25=
NM_001354800.1:c.73C>T NP_001341729.1:p.Leu25=
NM_033507.2:c.76C>T NP_277042.1:p.Leu26=
NM_033508.2:c.70C>T NP_277043.1:p.Leu24=
NM_000162.5:c.73C>T MANE Select NP_000153.1:p.Leu25=
NM_033507.3:c.76C>T NP_277042.1:p.Leu26=
NM_033508.3:c.70C>T NP_277043.1:p.Leu24=
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