Canonical Allele Identifier: CA367398639
Gene: GCK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145578T>G , CM000669.2:g.44145578T>G GRCh38
NC_000007.13:g.44185177T>G , CM000669.1:g.44185177T>G GRCh37
NC_000007.12:g.44151702T>G NCBI36
NG_008847.1:g.48846A>C
NG_008847.2:g.57593A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1170A>C ENSP00000379142.4:n.*1170A>C
ENST00000616242.5:c.*292A>C ENSP00000482149.2:n.*292A>C
ENST00000683378.1:n.398A>C
ENST00000336642.9:c.206A>C ENSP00000338009.5:p.Asn69Thr
ENST00000345378.7:c.1175A>C ENSP00000223366.2:p.Asn392Thr
ENST00000403799.8:c.1172A>C MANE Select ENSP00000384247.3:p.Asn391Thr
ENST00000671824.1:c.1235A>C ENSP00000500264.1:p.Asn412Thr
ENST00000672743.1:n.184A>C
ENST00000673284.1:c.1172A>C ENSP00000499852.1:p.Asn391Thr
ENST00000336642.8:c.224A>C ENSP00000338009.4:p.Asn75Thr
ENST00000345378.6:c.1175A>C ENSP00000223366.2:p.Asn392Thr
ENST00000395796.7:c.1169A>C ENSP00000379142.3:p.Asn390Thr
ENST00000403799.7:c.1172A>C ENSP00000384247.3:p.Asn391Thr
ENST00000437084.1:c.1121A>C ENSP00000402840.1:p.Asn374Thr
ENST00000459642.1:n.552A>C
ENST00000616242.4:c.1169A>C ENSP00000482149.1:p.Asn390Thr
NM_000162.3:c.1172A>C NP_000153.1:p.Asn391Thr
NM_033507.1:c.1175A>C NP_277042.1:p.Asn392Thr
NM_033508.1:c.1169A>C NP_277043.1:p.Asn390Thr
NM_000162.4:c.1172A>C NP_000153.1:p.Asn391Thr
NM_001354800.1:c.1172A>C NP_001341729.1:p.Asn391Thr
NM_001354801.1:c.161A>C NP_001341730.1:p.Asn54Thr
NM_001354802.1:c.32A>C NP_001341731.1:p.Asn11Thr
NM_001354803.1:c.206A>C NP_001341732.1:p.Asn69Thr
NM_033507.2:c.1175A>C NP_277042.1:p.Asn392Thr
NM_033508.2:c.1169A>C NP_277043.1:p.Asn390Thr
XM_024446707.1:c.32A>C XP_024302475.1:p.Asn11Thr
NM_000162.5:c.1172A>C MANE Select NP_000153.1:p.Asn391Thr
NM_033507.3:c.1175A>C NP_277042.1:p.Asn392Thr
NM_033508.3:c.1169A>C NP_277043.1:p.Asn390Thr
NM_001354803.2:c.206A>C NP_001341732.1:p.Asn69Thr