Canonical Allele Identifier: CA1139771162
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44148538_44152555dup , CM000669.2:g.44148538_44152555dup GRCh38
NC_000007.13:g.44188137_44192154dup , CM000669.1:g.44188137_44192154dup GRCh37
NC_000007.12:g.44154662_44158679dup NCBI36
NG_008847.1:g.41869_45886dup
NG_008847.2:g.50616_54633dup

Transcript Alleles

HGVS Amino-acid change
ENST00000395796.8:c.*207-130_*678-705dup
ENST00000616242.5:c.209-130_680-705dup
ENST00000682635.1:n.695-130_2387dup
ENST00000345378.7:c.212-130_683-705dup
ENST00000403799.8:c.209-130_680-705dup
ENST00000671824.1:c.209-130_680-705dup
ENST00000673284.1:c.209-130_680-705dup
ENST00000345378.6:c.212-130_683-705dup
ENST00000395796.7:c.206-130_677-705dup
ENST00000403799.7:c.209-130_680-705dup
ENST00000437084.1:c.209-130_629-705dup
ENST00000616242.4:n.206-130_677-705dup
NM_000162.3:c.209-130_680-705dup
NM_033507.1:c.212-130_683-705dup
NM_033508.1:c.206-130_677-705dup
NM_000162.4:c.209-130_680-705dup
NM_001354800.1:c.209-130_680-705dup
NM_033507.2:c.212-130_683-705dup
NM_033508.2:c.206-130_677-705dup
NM_000162.5:c.209-130_680-705dup
NM_033507.3:c.212-130_683-705dup
NM_033508.3:c.206-130_677-705dup