Canonical Allele Identifier: CA1703612962
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145701T= , CM000669.2:g.44145701T= GRCh38
NC_000007.13:g.44185300T= , CM000669.1:g.44185300T= GRCh37
NC_000007.12:g.44151825T= NCBI36
NG_008847.1:g.48723A=
NG_008847.2:g.57470A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1047A= ENSP00000379142.4:n.*1047A=
ENST00000616242.5:c.*169A= ENSP00000482149.2:n.*169A=
ENST00000683378.1:n.275A=
ENST00000336642.9:c.83A= ENSP00000338009.5:p.Asn28=
ENST00000345378.7:c.1052A= ENSP00000223366.2:p.Asn351=
ENST00000403799.8:c.1049A= MANE Select ENSP00000384247.3:p.Asn350=
ENST00000671824.1:c.1112A= ENSP00000500264.1:p.Asn371=
ENST00000672743.1:n.61A=
ENST00000673284.1:c.1049A= ENSP00000499852.1:p.Asn350=
ENST00000336642.8:c.101A= ENSP00000338009.4:p.Asn34=
ENST00000345378.6:c.1052A= ENSP00000223366.2:p.Asn351=
ENST00000395796.7:c.1046A= ENSP00000379142.3:p.Asn349=
ENST00000403799.7:c.1049A= ENSP00000384247.3:p.Asn350=
ENST00000437084.1:c.998A= ENSP00000402840.1:p.Asn333=
ENST00000459642.1:n.429A=
ENST00000473353.1:n.347A=
ENST00000616242.4:c.1046A= ENSP00000482149.1:p.Asn349=
NM_000162.3:c.1049A= NP_000153.1:p.Asn350=
NM_033507.1:c.1052A= NP_277042.1:p.Asn351=
NM_033508.1:c.1046A= NP_277043.1:p.Asn349=
NM_000162.4:c.1049A= NP_000153.1:p.Asn350=
NM_001354800.1:c.1049A= NP_001341729.1:p.Asn350=
NM_001354801.1:c.38A= NP_001341730.1:p.Asn13=
NM_001354802.1:c.-92A= NP_001341731.1:n.-92A=
NM_001354803.1:c.83A= NP_001341732.1:p.Asn28=
NM_033507.2:c.1052A= NP_277042.1:p.Asn351=
NM_033508.2:c.1046A= NP_277043.1:p.Asn349=
XM_024446707.1:c.-92A= XP_024302475.1:n.-92A=
NM_000162.5:c.1049A= MANE Select NP_000153.1:p.Asn350=
NM_033507.3:c.1052A= NP_277042.1:p.Asn351=
NM_033508.3:c.1046A= NP_277043.1:p.Asn349=
NM_001354803.2:c.83A= NP_001341732.1:p.Asn28=