Canonical Allele Identifier: CA2682589710
Gene: GCK HGNC NCBI

Linked Data

gnomAD v4: 7-44147970-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44147970T>A , CM000669.2:g.44147970T>A GRCh38
NC_000007.13:g.44187569T>A , CM000669.1:g.44187569T>A GRCh37
NC_000007.12:g.44154094T>A NCBI36
NG_008847.1:g.46454A>T
NG_008847.2:g.55201A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*678-137A>T ENSP00000379142.4:n.*678-137A>T
ENST00000616242.5:c.680-137A>T ENSP00000482149.2:n.680-137A>T
ENST00000345378.7:c.683-137A>T ENSP00000223366.2:n.683-137A>T
ENST00000403799.8:c.680-137A>T MANE Select ENSP00000384247.3:n.680-137A>T
ENST00000671824.1:c.680-137A>T ENSP00000500264.1:n.680-137A>T
ENST00000673284.1:c.680-137A>T ENSP00000499852.1:n.680-137A>T
ENST00000345378.6:c.683-137A>T ENSP00000223366.2:n.683-137A>T
ENST00000395796.7:c.677-137A>T ENSP00000379142.3:n.677-137A>T
ENST00000403799.7:c.680-137A>T ENSP00000384247.3:n.680-137A>T
ENST00000437084.1:c.629-137A>T ENSP00000402840.1:n.629-137A>T
ENST00000616242.4:c.677-137A>T ENSP00000482149.1:n.677-137A>T
NM_000162.3:c.680-137A>T NP_000153.1:n.680-137A>T
NM_033507.1:c.683-137A>T NP_277042.1:n.683-137A>T
NM_033508.1:c.677-137A>T NP_277043.1:n.677-137A>T
XR_927223.1:n.82+222T>A
NM_000162.4:c.680-137A>T NP_000153.1:n.680-137A>T
NM_001354800.1:c.680-137A>T NP_001341729.1:n.680-137A>T
NM_033507.2:c.683-137A>T NP_277042.1:n.683-137A>T
NM_033508.2:c.677-137A>T NP_277043.1:n.677-137A>T
XR_927223.2:n.82+222T>A
NM_000162.5:c.680-137A>T MANE Select NP_000153.1:n.680-137A>T
NM_033507.3:c.683-137A>T NP_277042.1:n.683-137A>T
NM_033508.3:c.677-137A>T NP_277043.1:n.677-137A>T
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