Canonical Allele Identifier: CA367398635
Gene: GCK HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1170A>T ENSP00000379142.4:n.*1170A>T
ENST00000616242.5:c.*292A>T ENSP00000482149.2:n.*292A>T
ENST00000683378.1:n.398A>T
ENST00000336642.9:c.206A>T ENSP00000338009.5:p.Asn69Ile
ENST00000345378.7:c.1175A>T ENSP00000223366.2:p.Asn392Ile
ENST00000403799.8:c.1172A>T MANE Select ENSP00000384247.3:p.Asn391Ile
ENST00000671824.1:c.1235A>T ENSP00000500264.1:p.Asn412Ile
ENST00000672743.1:n.184A>T
ENST00000673284.1:c.1172A>T ENSP00000499852.1:p.Asn391Ile
ENST00000336642.8:c.224A>T ENSP00000338009.4:p.Asn75Ile
ENST00000345378.6:c.1175A>T ENSP00000223366.2:p.Asn392Ile
ENST00000395796.7:c.1169A>T ENSP00000379142.3:p.Asn390Ile
ENST00000403799.7:c.1172A>T ENSP00000384247.3:p.Asn391Ile
ENST00000437084.1:c.1121A>T ENSP00000402840.1:p.Asn374Ile
ENST00000459642.1:n.552A>T
ENST00000616242.4:c.1169A>T ENSP00000482149.1:p.Asn390Ile
NM_000162.3:c.1172A>T NP_000153.1:p.Asn391Ile
NM_033507.1:c.1175A>T NP_277042.1:p.Asn392Ile
NM_033508.1:c.1169A>T NP_277043.1:p.Asn390Ile
NM_000162.4:c.1172A>T NP_000153.1:p.Asn391Ile
NM_001354800.1:c.1172A>T NP_001341729.1:p.Asn391Ile
NM_001354801.1:c.161A>T NP_001341730.1:p.Asn54Ile
NM_001354802.1:c.32A>T NP_001341731.1:p.Asn11Ile
NM_001354803.1:c.206A>T NP_001341732.1:p.Asn69Ile
NM_033507.2:c.1175A>T NP_277042.1:p.Asn392Ile
NM_033508.2:c.1169A>T NP_277043.1:p.Asn390Ile
XM_024446707.1:c.32A>T XP_024302475.1:p.Asn11Ile
NM_000162.5:c.1172A>T MANE Select NP_000153.1:p.Asn391Ile
NM_033507.3:c.1175A>T NP_277042.1:p.Asn392Ile
NM_033508.3:c.1169A>T NP_277043.1:p.Asn390Ile
NM_001354803.2:c.206A>T NP_001341732.1:p.Asn69Ile