Canonical Allele Identifier: CA1703653824
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44189371C= , CM000669.2:g.44189371C= GRCh38
NC_000007.13:g.44228970C= , CM000669.1:g.44228970C= GRCh37
NC_000007.12:g.44195495C= NCBI36
NG_008847.1:g.5053G=
NG_008847.2:g.13800G=

Transcript Alleles

HGVS Amino-acid change
ENST00000616242.5:c.-418G= ENSP00000482149.2:n.-418G=
ENST00000682635.1:n.69G=
ENST00000403799.8:c.-418G= MANE Select ENSP00000384247.3:n.-418G=
ENST00000671824.1:c.-418G= ENSP00000500264.1:n.-418G=
ENST00000673284.1:c.-418G= ENSP00000499852.1:n.-418G=
ENST00000403799.7:c.-418G= ENSP00000384247.3:n.-418G=
ENST00000476008.1:n.480+8320G=
NM_000162.3:c.-418G= NP_000153.1:n.-418G=
NM_000162.4:c.-418G= NP_000153.1:n.-418G=
NM_001354800.1:c.-418G= NP_001341729.1:n.-418G=
NM_000162.5:c.-418G= MANE Select NP_000153.1:n.-418G=