Canonical Allele Identifier: CA3004402265
Community Standard Title: NC_000007.14:g.44150065dup
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44150065dup , CM000669.2:g.44150065dup GRCh38
NC_000007.13:g.44189664dup , CM000669.1:g.44189664dup GRCh37
NC_000007.12:g.44156189dup NCBI36
NG_008847.1:g.44361dup
NG_008847.2:g.53108dup

Transcript Alleles

HGVS Amino-acid Change
NM_000162.3:c.485dup
NM_000162.4:c.485dup
NM_000162.5:c.485dup
NM_001354800.1:c.485dup
NM_033507.1:c.488dup
NM_033507.2:c.488dup
NM_033507.3:c.488dup
NM_033508.1:c.482dup
NM_033508.2:c.482dup
NM_033508.3:c.482dup
ENST00000345378.6:c.488dup
ENST00000345378.7:c.488dup
ENST00000395796.7:c.482dup
ENST00000395796.8:c.*483dup
ENST00000403799.7:c.485dup
ENST00000403799.8:c.485dup
ENST00000437084.1:c.434dup
ENST00000616242.4:c.482dup
ENST00000616242.5:c.485dup
ENST00000671824.1:c.485dup
ENST00000673284.1:c.485dup
ENST00000682635.1:n.971dup