Canonical Allele Identifier: CA1703637529
Gene: GCK HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44153347A= , CM000669.2:g.44153347A= GRCh38
NC_000007.13:g.44192946A= , CM000669.1:g.44192946A= GRCh37
NC_000007.12:g.44159471A= NCBI36
NG_008847.1:g.41077T=
NG_008847.2:g.49824T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*160T= ENSP00000379142.4:n.*160T=
ENST00000616242.5:c.162T= ENSP00000482149.2:p.Ser54=
ENST00000682635.1:n.648T=
ENST00000345378.7:c.165T= ENSP00000223366.2:p.Ser55=
ENST00000403799.8:c.162T= MANE Select ENSP00000384247.3:p.Ser54=
ENST00000671824.1:c.162T= ENSP00000500264.1:p.Ser54=
ENST00000673284.1:c.162T= ENSP00000499852.1:p.Ser54=
ENST00000345378.6:c.165T= ENSP00000223366.2:p.Ser55=
ENST00000395796.7:c.159T= ENSP00000379142.3:p.Ser53=
ENST00000403799.7:c.162T= ENSP00000384247.3:p.Ser54=
ENST00000437084.1:c.162T= ENSP00000402840.1:p.Ser54=
ENST00000616242.4:c.159T= ENSP00000482149.1:p.Ser53=
NM_000162.3:c.162T= NP_000153.1:p.Ser54=
NM_033507.1:c.165T= NP_277042.1:p.Ser55=
NM_033508.1:c.159T= NP_277043.1:p.Ser53=
NM_000162.4:c.162T= NP_000153.1:p.Ser54=
NM_001354800.1:c.162T= NP_001341729.1:p.Ser54=
NM_033507.2:c.165T= NP_277042.1:p.Ser55=
NM_033508.2:c.159T= NP_277043.1:p.Ser53=
NM_000162.5:c.162T= MANE Select NP_000153.1:p.Ser54=
NM_033507.3:c.165T= NP_277042.1:p.Ser55=
NM_033508.3:c.159T= NP_277043.1:p.Ser53=
Search 100 bp 5'
Search 100 bp 3'