Canonical Allele Identifier: CA454610682
Gene: GCK HGNC NCBI

Linked Data

gnomAD v4: 7-44153455-C-T
MyVariant Identifiers: chr7:g.44193054C>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44153455C>T , CM000669.2:g.44153455C>T GRCh38
NC_000007.13:g.44193054C>T , CM000669.1:g.44193054C>T GRCh37
NC_000007.12:g.44159579C>T NCBI36
NG_008847.1:g.40969G>A
NG_008847.2:g.49716G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*52G>A ENSP00000379142.4:n.*52G>A
ENST00000616242.5:c.54G>A ENSP00000482149.2:p.Gln18=
ENST00000682635.1:n.540G>A
ENST00000345378.7:c.57G>A ENSP00000223366.2:p.Gln19=
ENST00000403799.8:c.54G>A MANE Select ENSP00000384247.3:p.Gln18=
ENST00000671824.1:c.54G>A ENSP00000500264.1:p.Gln18=
ENST00000673284.1:c.54G>A ENSP00000499852.1:p.Gln18=
ENST00000345378.6:c.57G>A ENSP00000223366.2:p.Gln19=
ENST00000395796.7:c.51G>A ENSP00000379142.3:p.Gln17=
ENST00000403799.7:c.54G>A ENSP00000384247.3:p.Gln18=
ENST00000437084.1:c.54G>A ENSP00000402840.1:p.Gln18=
ENST00000476008.1:n.489G>A
ENST00000616242.4:c.51G>A ENSP00000482149.1:p.Gln17=
NM_000162.3:c.54G>A NP_000153.1:p.Gln18=
NM_033507.1:c.57G>A NP_277042.1:p.Gln19=
NM_033508.1:c.51G>A NP_277043.1:p.Gln17=
NM_000162.4:c.54G>A NP_000153.1:p.Gln18=
NM_001354800.1:c.54G>A NP_001341729.1:p.Gln18=
NM_033507.2:c.57G>A NP_277042.1:p.Gln19=
NM_033508.2:c.51G>A NP_277043.1:p.Gln17=
NM_000162.5:c.54G>A MANE Select NP_000153.1:p.Gln18=
NM_033507.3:c.57G>A NP_277042.1:p.Gln19=
NM_033508.3:c.51G>A NP_277043.1:p.Gln17=
Search 100 bp 5'
Search 100 bp 3'