Canonical Allele Identifier: CA213779
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 36214
dbSNP Id: rs193922293

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44151116dup , CM000669.2:g.44151116dup GRCh38
NC_000007.13:g.44190715dup , CM000669.1:g.44190715dup GRCh37
NC_000007.12:g.44157240dup NCBI36
NG_008847.1:g.43314dup
NG_008847.2:g.52061dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*362-35dup ENSP00000379142.4:n.*362-35dup
ENST00000616242.5:c.364-35dup ENSP00000482149.2:n.364-35dup
ENST00000682635.1:n.850-35dup
ENST00000345378.7:c.367-35dup ENSP00000223366.2:n.367-35dup
ENST00000403799.8:c.364-35dup MANE Select ENSP00000384247.3:n.364-35dup
ENST00000671824.1:c.364-35dup ENSP00000500264.1:n.364-35dup
ENST00000673284.1:c.364-35dup ENSP00000499852.1:n.364-35dup
ENST00000345378.6:c.367-35dup ENSP00000223366.2:n.367-35dup
ENST00000395796.7:c.361-35dup ENSP00000379142.3:n.361-35dup
ENST00000403799.7:c.364-35dup ENSP00000384247.3:n.364-35dup
ENST00000437084.1:c.364-86dup ENSP00000402840.1:n.364-86dup
ENST00000616242.4:c.361-35dup ENSP00000482149.1:n.361-35dup
NM_000162.3:c.364-35dup NP_000153.1:n.364-35dup
NM_033507.1:c.367-35dup NP_277042.1:n.367-35dup
NM_033508.1:c.361-35dup NP_277043.1:n.361-35dup
NM_000162.4:c.364-35dup NP_000153.1:n.364-35dup
NM_001354800.1:c.364-35dup NP_001341729.1:n.364-35dup
NM_033507.2:c.367-35dup NP_277042.1:n.367-35dup
NM_033508.2:c.361-35dup NP_277043.1:n.361-35dup
NM_000162.5:c.364-35dup MANE Select NP_000153.1:n.364-35dup
NM_033507.3:c.367-35dup NP_277042.1:n.367-35dup
NM_033508.3:c.361-35dup NP_277043.1:n.361-35dup