Canonical Allele Identifier: CA2578878533
Gene: GCK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44153226del , CM000669.2:g.44153226del GRCh38
NC_000007.13:g.44192825del , CM000669.1:g.44192825del GRCh37
NC_000007.12:g.44159350del NCBI36
NG_008847.1:g.41198del
NG_008847.2:g.49945del

Transcript Alleles

HGVS Amino-acid change
ENST00000395796.8:c.*206+75del ENSP00000379142.4:n.*206+75del
ENST00000616242.5:c.208+75del ENSP00000482149.2:n.208+75del
ENST00000682635.1:n.694+75del
ENST00000345378.7:c.211+75del ENSP00000223366.2:n.211+75del
ENST00000403799.8:c.208+75del MANE Select ENSP00000384247.3:n.208+75del
ENST00000671824.1:c.208+75del ENSP00000500264.1:n.208+75del
ENST00000673284.1:c.208+75del ENSP00000499852.1:n.208+75del
ENST00000345378.6:c.211+75del ENSP00000223366.2:n.211+75del
ENST00000395796.7:c.205+75del ENSP00000379142.3:n.205+75del
ENST00000403799.7:c.208+75del ENSP00000384247.3:n.208+75del
ENST00000437084.1:c.208+75del ENSP00000402840.1:n.208+75del
ENST00000616242.4:c.205+75del ENSP00000482149.1:n.205+75del
NM_000162.3:c.208+75del NP_000153.1:n.208+75del
NM_033507.1:c.211+75del NP_277042.1:n.211+75del
NM_033508.1:c.205+75del NP_277043.1:n.205+75del
NM_000162.4:c.208+75del NP_000153.1:n.208+75del
NM_001354800.1:c.208+75del NP_001341729.1:n.208+75del
NM_033507.2:c.211+75del NP_277042.1:n.211+75del
NM_033508.2:c.205+75del NP_277043.1:n.205+75del
NM_000162.5:c.208+75del MANE Select NP_000153.1:n.208+75del
NM_033507.3:c.211+75del NP_277042.1:n.211+75del
NM_033508.3:c.205+75del NP_277043.1:n.205+75del