Canonical Allele Identifier: CA573798431
Gene: GCK HGNC NCBI

Linked Data

dbSNP Id: rs1302090948
gnomAD v2: 7-44190678-G-A
gnomAD v4: 7-44151079-G-A
MyVariant Identifiers: chr7:g.44190678G>A (hg19) chr7:g.44151079G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44151079G>A , CM000669.2:g.44151079G>A GRCh38
NC_000007.13:g.44190678G>A , CM000669.1:g.44190678G>A GRCh37
NC_000007.12:g.44157203G>A NCBI36
NG_008847.1:g.43345C>T
NG_008847.2:g.52092C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*362-4C>T ENSP00000379142.4:n.*362-4C>T
ENST00000616242.5:c.364-4C>T ENSP00000482149.2:n.364-4C>T
ENST00000682635.1:n.850-4C>T
ENST00000345378.7:c.367-4C>T ENSP00000223366.2:n.367-4C>T
ENST00000403799.8:c.364-4C>T MANE Select ENSP00000384247.3:n.364-4C>T
ENST00000671824.1:c.364-4C>T ENSP00000500264.1:n.364-4C>T
ENST00000673284.1:c.364-4C>T ENSP00000499852.1:n.364-4C>T
ENST00000345378.6:c.367-4C>T ENSP00000223366.2:n.367-4C>T
ENST00000395796.7:c.361-4C>T ENSP00000379142.3:n.361-4C>T
ENST00000403799.7:c.364-4C>T ENSP00000384247.3:n.364-4C>T
ENST00000437084.1:c.364-55C>T ENSP00000402840.1:n.364-55C>T
ENST00000616242.4:c.361-4C>T ENSP00000482149.1:n.361-4C>T
NM_000162.3:c.364-4C>T NP_000153.1:n.364-4C>T
NM_033507.1:c.367-4C>T NP_277042.1:n.367-4C>T
NM_033508.1:c.361-4C>T NP_277043.1:n.361-4C>T
NM_000162.4:c.364-4C>T NP_000153.1:n.364-4C>T
NM_001354800.1:c.364-4C>T NP_001341729.1:n.364-4C>T
NM_033507.2:c.367-4C>T NP_277042.1:n.367-4C>T
NM_033508.2:c.361-4C>T NP_277043.1:n.361-4C>T
NM_000162.5:c.364-4C>T MANE Select NP_000153.1:n.364-4C>T
NM_033507.3:c.367-4C>T NP_277042.1:n.367-4C>T
NM_033508.3:c.361-4C>T NP_277043.1:n.361-4C>T
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