Canonical Allele Identifier: CA2695203141
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44149860del , CM000669.2:g.44149860del GRCh38
NC_000007.13:g.44189459del , CM000669.1:g.44189459del GRCh37
NC_000007.12:g.44155984del NCBI36
NG_008847.1:g.44565del
NG_008847.2:g.53312del

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*578del
ENST00000616242.5:c.580del
ENST00000682635.1:n.1066del
ENST00000345378.7:c.583del
ENST00000403799.8:c.580del
ENST00000671824.1:c.580del
ENST00000673284.1:c.580del
ENST00000345378.6:c.583del
ENST00000395796.7:c.577del
ENST00000403799.7:c.580del
ENST00000437084.1:c.529del
ENST00000616242.4:c.577del
NM_000162.3:c.580del
NM_033507.1:c.583del
NM_033508.1:c.577del
NM_000162.4:c.580del
NM_001354800.1:c.580del
NM_033507.2:c.583del
NM_033508.2:c.577del
NM_000162.5:c.580del
NM_033507.3:c.583del
NM_033508.3:c.577del