Canonical Allele Identifier: CA1703612943
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145661G= , CM000669.2:g.44145661G= GRCh38
NC_000007.13:g.44185260G= , CM000669.1:g.44185260G= GRCh37
NC_000007.12:g.44151785G= NCBI36
NG_008847.1:g.48763C=
NG_008847.2:g.57510C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1087C= ENSP00000379142.4:n.*1087C=
ENST00000616242.5:c.*209C= ENSP00000482149.2:n.*209C=
ENST00000683378.1:n.315C=
ENST00000336642.9:c.123C= ENSP00000338009.5:p.Asp41=
ENST00000345378.7:c.1092C= ENSP00000223366.2:p.Asp364=
ENST00000403799.8:c.1089C= MANE Select ENSP00000384247.3:p.Asp363=
ENST00000671824.1:c.1152C= ENSP00000500264.1:p.Asp384=
ENST00000672743.1:n.101C=
ENST00000673284.1:c.1089C= ENSP00000499852.1:p.Asp363=
ENST00000336642.8:c.141C= ENSP00000338009.4:p.Asp47=
ENST00000345378.6:c.1092C= ENSP00000223366.2:p.Asp364=
ENST00000395796.7:c.1086C= ENSP00000379142.3:p.Asp362=
ENST00000403799.7:c.1089C= ENSP00000384247.3:p.Asp363=
ENST00000437084.1:c.1038C= ENSP00000402840.1:p.Asp346=
ENST00000459642.1:n.469C=
ENST00000473353.1:n.387C=
ENST00000616242.4:c.1086C= ENSP00000482149.1:p.Asp362=
NM_000162.3:c.1089C= NP_000153.1:p.Asp363=
NM_033507.1:c.1092C= NP_277042.1:p.Asp364=
NM_033508.1:c.1086C= NP_277043.1:p.Asp362=
NM_000162.4:c.1089C= NP_000153.1:p.Asp363=
NM_001354800.1:c.1089C= NP_001341729.1:p.Asp363=
NM_001354801.1:c.78C= NP_001341730.1:p.Asp26=
NM_001354802.1:c.-52C= NP_001341731.1:n.-52C=
NM_001354803.1:c.123C= NP_001341732.1:p.Asp41=
NM_033507.2:c.1092C= NP_277042.1:p.Asp364=
NM_033508.2:c.1086C= NP_277043.1:p.Asp362=
XM_024446707.1:c.-52C= XP_024302475.1:n.-52C=
NM_000162.5:c.1089C= MANE Select NP_000153.1:p.Asp363=
NM_033507.3:c.1092C= NP_277042.1:p.Asp364=
NM_033508.3:c.1086C= NP_277043.1:p.Asp362=
NM_001354803.2:c.123C= NP_001341732.1:p.Asp41=