Canonical Allele Identifier: CA1703653827
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44189375T= , CM000669.2:g.44189375T= GRCh38
NC_000007.13:g.44228974T= , CM000669.1:g.44228974T= GRCh37
NC_000007.12:g.44195499T= NCBI36
NG_008847.1:g.5049A=
NG_008847.2:g.13796A=

Transcript Alleles

HGVS Amino-acid change
ENST00000616242.5:c.-422A= ENSP00000482149.2:n.-422A=
ENST00000682635.1:n.65A=
ENST00000403799.8:c.-422A= MANE Select ENSP00000384247.3:n.-422A=
ENST00000671824.1:c.-422A= ENSP00000500264.1:n.-422A=
ENST00000673284.1:c.-422A= ENSP00000499852.1:n.-422A=
ENST00000403799.7:c.-422A= ENSP00000384247.3:n.-422A=
ENST00000476008.1:n.480+8316A=
NM_000162.3:c.-422A= NP_000153.1:n.-422A=
NM_000162.4:c.-422A= NP_000153.1:n.-422A=
NM_001354800.1:c.-422A= NP_001341729.1:n.-422A=
NM_000162.5:c.-422A= MANE Select NP_000153.1:n.-422A=