Canonical Allele Identifier: CA2697557255
Gene: GCK HGNC NCBI

Linked Data

ClinVar Variation Id: 2684207
ClinVar RCV Id: RCV003482703

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44153459_44153467del , CM000669.2:g.44153459_44153467del GRCh38
NC_000007.13:g.44193058_44193066del , CM000669.1:g.44193058_44193066del GRCh37
NC_000007.12:g.44159583_44159591del NCBI36
NG_008847.1:g.40961_40969del
NG_008847.2:g.49708_49716del

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*44_*52del
ENST00000616242.5:c.46_54del
ENST00000682635.1:n.532_540del
ENST00000345378.7:c.49_57del
ENST00000403799.8:c.46_54del
ENST00000671824.1:c.46_54del
ENST00000673284.1:c.46_54del
ENST00000345378.6:c.49_57del
ENST00000395796.7:c.43_51del
ENST00000403799.7:c.46_54del
ENST00000437084.1:c.46_54del
ENST00000476008.1:n.481_489del
ENST00000616242.4:c.43_51del
NM_000162.3:c.46_54del
NM_033507.1:c.49_57del
NM_033508.1:c.43_51del
NM_000162.4:c.46_54del
NM_001354800.1:c.46_54del
NM_033507.2:c.49_57del
NM_033508.2:c.43_51del
NM_000162.5:c.46_54del
NM_033507.3:c.49_57del
NM_033508.3:c.43_51del