Canonical Allele Identifier: CA2682574984
Gene: GCK HGNC NCBI

Linked Data

gnomAD v4: 7-44189389-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44189389C>T , CM000669.2:g.44189389C>T GRCh38
NC_000007.13:g.44228988C>T , CM000669.1:g.44228988C>T GRCh37
NC_000007.12:g.44195513C>T NCBI36
NG_008847.1:g.5035G>A
NG_008847.2:g.13782G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000616242.5:c.-436G>A ENSP00000482149.2:n.-436G>A
ENST00000682635.1:n.51G>A
ENST00000403799.8:c.-436G>A MANE Select ENSP00000384247.3:n.-436G>A
ENST00000671824.1:c.-436G>A ENSP00000500264.1:n.-436G>A
ENST00000673284.1:c.-436G>A ENSP00000499852.1:n.-436G>A
ENST00000403799.7:c.-436G>A ENSP00000384247.3:n.-436G>A
ENST00000476008.1:n.480+8302G>A
NM_000162.3:c.-436G>A NP_000153.1:n.-436G>A
NM_000162.4:c.-436G>A NP_000153.1:n.-436G>A
NM_001354800.1:c.-436G>A NP_001341729.1:n.-436G>A
NM_000162.5:c.-436G>A MANE Select NP_000153.1:n.-436G>A
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