Canonical Allele Identifier: CA1703653829
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44189379A= , CM000669.2:g.44189379A= GRCh38
NC_000007.13:g.44228978A= , CM000669.1:g.44228978A= GRCh37
NC_000007.12:g.44195503A= NCBI36
NG_008847.1:g.5045T=
NG_008847.2:g.13792T=

Transcript Alleles

HGVS Amino-acid change
ENST00000616242.5:c.-426T= ENSP00000482149.2:n.-426T=
ENST00000682635.1:n.61T=
ENST00000403799.8:c.-426T= MANE Select ENSP00000384247.3:n.-426T=
ENST00000671824.1:c.-426T= ENSP00000500264.1:n.-426T=
ENST00000673284.1:c.-426T= ENSP00000499852.1:n.-426T=
ENST00000403799.7:c.-426T= ENSP00000384247.3:n.-426T=
ENST00000476008.1:n.480+8312T=
NM_000162.3:c.-426T= NP_000153.1:n.-426T=
NM_000162.4:c.-426T= NP_000153.1:n.-426T=
NM_001354800.1:c.-426T= NP_001341729.1:n.-426T=
NM_000162.5:c.-426T= MANE Select NP_000153.1:n.-426T=