Canonical Allele Identifier: CA454608697
Gene: GCK HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.44187326G>A (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44147727G>A , CM000669.2:g.44147727G>A GRCh38
NC_000007.13:g.44187326G>A , CM000669.1:g.44187326G>A GRCh37
NC_000007.12:g.44153851G>A NCBI36
NG_008847.1:g.46697C>T
NG_008847.2:g.55444C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*784C>T ENSP00000379142.4:n.*784C>T
ENST00000616242.5:c.786C>T ENSP00000482149.2:p.Asp262=
ENST00000345378.7:c.789C>T ENSP00000223366.2:p.Asp263=
ENST00000403799.8:c.786C>T MANE Select ENSP00000384247.3:p.Asp262=
ENST00000671824.1:c.786C>T ENSP00000500264.1:p.Asp262=
ENST00000673284.1:c.786C>T ENSP00000499852.1:p.Asp262=
ENST00000345378.6:c.789C>T ENSP00000223366.2:p.Asp263=
ENST00000395796.7:c.783C>T ENSP00000379142.3:p.Asp261=
ENST00000403799.7:c.786C>T ENSP00000384247.3:p.Asp262=
ENST00000437084.1:c.735C>T ENSP00000402840.1:p.Asp245=
ENST00000616242.4:c.783C>T ENSP00000482149.1:p.Asp261=
NM_000162.3:c.786C>T NP_000153.1:p.Asp262=
NM_033507.1:c.789C>T NP_277042.1:p.Asp263=
NM_033508.1:c.783C>T NP_277043.1:p.Asp261=
XR_927223.1:n.61G>A
NM_000162.4:c.786C>T NP_000153.1:p.Asp262=
NM_001354800.1:c.786C>T NP_001341729.1:p.Asp262=
NM_033507.2:c.789C>T NP_277042.1:p.Asp263=
NM_033508.2:c.783C>T NP_277043.1:p.Asp261=
XR_927223.2:n.61G>A
NM_000162.5:c.786C>T MANE Select NP_000153.1:p.Asp262=
NM_033507.3:c.789C>T NP_277042.1:p.Asp263=
NM_033508.3:c.783C>T NP_277043.1:p.Asp261=
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