Canonical Allele Identifier: CA367396799
Gene: GCK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145157C>G , CM000669.2:g.44145157C>G GRCh38
NC_000007.13:g.44184756C>G , CM000669.1:g.44184756C>G GRCh37
NC_000007.12:g.44151281C>G NCBI36
NG_008847.1:g.49267G>C
NG_008847.2:g.58014G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1375G>C ENSP00000379142.4:n.*1375G>C
ENST00000616242.5:c.*497G>C ENSP00000482149.2:n.*497G>C
ENST00000683378.1:n.603G>C
ENST00000336642.9:c.411G>C ENSP00000338009.5:p.Lys137Asn
ENST00000345378.7:c.1380G>C ENSP00000223366.2:p.Lys460Asn
ENST00000403799.8:c.1377G>C MANE Select ENSP00000384247.3:p.Lys459Asn
ENST00000671824.1:c.1440G>C ENSP00000500264.1:p.Lys480Asn
ENST00000672743.1:n.381+8G>C
ENST00000673284.1:c.1369+8G>C ENSP00000499852.1:n.1369+8G>C
ENST00000336642.8:c.429G>C ENSP00000338009.4:p.Lys143Asn
ENST00000345378.6:c.1380G>C ENSP00000223366.2:p.Lys460Asn
ENST00000395796.7:c.1374G>C ENSP00000379142.3:p.Lys458Asn
ENST00000403799.7:c.1377G>C ENSP00000384247.3:p.Lys459Asn
ENST00000437084.1:c.1326G>C ENSP00000402840.1:p.Lys442Asn
ENST00000459642.1:n.757G>C
ENST00000616242.4:c.1374G>C ENSP00000482149.1:p.Lys458Asn
NM_000162.3:c.1377G>C NP_000153.1:p.Lys459Asn
NM_033507.1:c.1380G>C NP_277042.1:p.Lys460Asn
NM_033508.1:c.1374G>C NP_277043.1:p.Lys458Asn
NM_000162.4:c.1377G>C NP_000153.1:p.Lys459Asn
NM_001354800.1:c.1369+8G>C NP_001341729.1:n.1369+8G>C
NM_001354801.1:c.366G>C NP_001341730.1:p.Lys122Asn
NM_001354802.1:c.229+8G>C NP_001341731.1:n.229+8G>C
NM_001354803.1:c.411G>C NP_001341732.1:p.Lys137Asn
NM_033507.2:c.1380G>C NP_277042.1:p.Lys460Asn
NM_033508.2:c.1374G>C NP_277043.1:p.Lys458Asn
XM_024446707.1:c.237G>C XP_024302475.1:p.Lys79Asn
NM_000162.5:c.1377G>C MANE Select NP_000153.1:p.Lys459Asn
NM_033507.3:c.1380G>C NP_277042.1:p.Lys460Asn
NM_033508.3:c.1374G>C NP_277043.1:p.Lys458Asn
NM_001354803.2:c.411G>C NP_001341732.1:p.Lys137Asn