Canonical Allele Identifier: CA2682575566
Gene: GCK HGNC NCBI

Linked Data

gnomAD v4: 7-44151108-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44151108A>T , CM000669.2:g.44151108A>T GRCh38
NC_000007.13:g.44190707A>T , CM000669.1:g.44190707A>T GRCh37
NC_000007.12:g.44157232A>T NCBI36
NG_008847.1:g.43316T>A
NG_008847.2:g.52063T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*362-33T>A ENSP00000379142.4:n.*362-33T>A
ENST00000616242.5:c.364-33T>A ENSP00000482149.2:n.364-33T>A
ENST00000682635.1:n.850-33T>A
ENST00000345378.7:c.367-33T>A ENSP00000223366.2:n.367-33T>A
ENST00000403799.8:c.364-33T>A MANE Select ENSP00000384247.3:n.364-33T>A
ENST00000671824.1:c.364-33T>A ENSP00000500264.1:n.364-33T>A
ENST00000673284.1:c.364-33T>A ENSP00000499852.1:n.364-33T>A
ENST00000345378.6:c.367-33T>A ENSP00000223366.2:n.367-33T>A
ENST00000395796.7:c.361-33T>A ENSP00000379142.3:n.361-33T>A
ENST00000403799.7:c.364-33T>A ENSP00000384247.3:n.364-33T>A
ENST00000437084.1:c.364-84T>A ENSP00000402840.1:n.364-84T>A
ENST00000616242.4:c.361-33T>A ENSP00000482149.1:n.361-33T>A
NM_000162.3:c.364-33T>A NP_000153.1:n.364-33T>A
NM_033507.1:c.367-33T>A NP_277042.1:n.367-33T>A
NM_033508.1:c.361-33T>A NP_277043.1:n.361-33T>A
NM_000162.4:c.364-33T>A NP_000153.1:n.364-33T>A
NM_001354800.1:c.364-33T>A NP_001341729.1:n.364-33T>A
NM_033507.2:c.367-33T>A NP_277042.1:n.367-33T>A
NM_033508.2:c.361-33T>A NP_277043.1:n.361-33T>A
NM_000162.5:c.364-33T>A MANE Select NP_000153.1:n.364-33T>A
NM_033507.3:c.367-33T>A NP_277042.1:n.367-33T>A
NM_033508.3:c.361-33T>A NP_277043.1:n.361-33T>A
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