Canonical Allele Identifier: CA2682588540
Gene: GCK HGNC NCBI

Linked Data

gnomAD v4: 7-44147542-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44147542C>G , CM000669.2:g.44147542C>G GRCh38
NC_000007.13:g.44187141C>G , CM000669.1:g.44187141C>G GRCh37
NC_000007.12:g.44153666C>G NCBI36
NG_008847.1:g.46882G>C
NG_008847.2:g.55629G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*861+108G>C ENSP00000379142.4:n.*861+108G>C
ENST00000616242.5:c.853+118G>C ENSP00000482149.2:n.853+118G>C
ENST00000345378.7:c.866+108G>C ENSP00000223366.2:n.866+108G>C
ENST00000403799.8:c.863+108G>C MANE Select ENSP00000384247.3:n.863+108G>C
ENST00000671824.1:c.853+118G>C ENSP00000500264.1:n.853+118G>C
ENST00000673284.1:c.863+108G>C ENSP00000499852.1:n.863+108G>C
ENST00000345378.6:c.866+108G>C ENSP00000223366.2:n.866+108G>C
ENST00000395796.7:c.860+108G>C ENSP00000379142.3:n.860+108G>C
ENST00000403799.7:c.863+108G>C ENSP00000384247.3:n.863+108G>C
ENST00000437084.1:c.812+108G>C ENSP00000402840.1:n.812+108G>C
ENST00000616242.4:c.860+108G>C ENSP00000482149.1:n.860+108G>C
NM_000162.3:c.863+108G>C NP_000153.1:n.863+108G>C
NM_033507.1:c.866+108G>C NP_277042.1:n.866+108G>C
NM_033508.1:c.860+108G>C NP_277043.1:n.860+108G>C
NM_000162.4:c.863+108G>C NP_000153.1:n.863+108G>C
NM_001354800.1:c.863+108G>C NP_001341729.1:n.863+108G>C
NM_033507.2:c.866+108G>C NP_277042.1:n.866+108G>C
NM_033508.2:c.860+108G>C NP_277043.1:n.860+108G>C
NM_000162.5:c.863+108G>C MANE Select NP_000153.1:n.863+108G>C
NM_033507.3:c.866+108G>C NP_277042.1:n.866+108G>C
NM_033508.3:c.860+108G>C NP_277043.1:n.860+108G>C
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