Canonical Allele Identifier: CA1703635884
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44149834A= , CM000669.2:g.44149834A= GRCh38
NC_000007.13:g.44189433A= , CM000669.1:g.44189433A= GRCh37
NC_000007.12:g.44155958A= NCBI36
NG_008847.1:g.44590T=
NG_008847.2:g.53337T=

Transcript Alleles

HGVS Amino-acid change
ENST00000395796.8:c.*603T= ENSP00000379142.4:n.*603T=
ENST00000616242.5:c.605T= ENSP00000482149.2:p.Met202=
ENST00000682635.1:n.1091T=
ENST00000345378.7:c.608T= ENSP00000223366.2:p.Met203=
ENST00000403799.8:c.605T= MANE Select ENSP00000384247.3:p.Met202=
ENST00000671824.1:c.605T= ENSP00000500264.1:p.Met202=
ENST00000673284.1:c.605T= ENSP00000499852.1:p.Met202=
ENST00000345378.6:c.608T= ENSP00000223366.2:p.Met203=
ENST00000395796.7:c.602T= ENSP00000379142.3:p.Met201=
ENST00000403799.7:c.605T= ENSP00000384247.3:p.Met202=
ENST00000437084.1:c.554T= ENSP00000402840.1:p.Met185=
ENST00000616242.4:n.602T= ENSP00000482149.1:p.Met201=
NM_000162.3:c.605T= NP_000153.1:p.Met202=
NM_033507.1:c.608T= NP_277042.1:p.Met203=
NM_033508.1:c.602T= NP_277043.1:p.Met201=
NM_000162.4:c.605T= NP_000153.1:p.Met202=
NM_001354800.1:c.605T= NP_001341729.1:p.Met202=
NM_033507.2:c.608T= NP_277042.1:p.Met203=
NM_033508.2:c.602T= NP_277043.1:p.Met201=
NM_000162.5:c.605T= MANE Select NP_000153.1:p.Met202=
NM_033507.3:c.608T= NP_277042.1:p.Met203=
NM_033508.3:c.602T= NP_277043.1:p.Met201=