Canonical Allele Identifier: CA367398642
Gene: GCK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145579T>A , CM000669.2:g.44145579T>A GRCh38
NC_000007.13:g.44185178T>A , CM000669.1:g.44185178T>A GRCh37
NC_000007.12:g.44151703T>A NCBI36
NG_008847.1:g.48845A>T
NG_008847.2:g.57592A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1169A>T ENSP00000379142.4:n.*1169A>T
ENST00000616242.5:c.*291A>T ENSP00000482149.2:n.*291A>T
ENST00000683378.1:n.397A>T
ENST00000336642.9:c.205A>T ENSP00000338009.5:p.Asn69Tyr
ENST00000345378.7:c.1174A>T ENSP00000223366.2:p.Asn392Tyr
ENST00000403799.8:c.1171A>T MANE Select ENSP00000384247.3:p.Asn391Tyr
ENST00000671824.1:c.1234A>T ENSP00000500264.1:p.Asn412Tyr
ENST00000672743.1:n.183A>T
ENST00000673284.1:c.1171A>T ENSP00000499852.1:p.Asn391Tyr
ENST00000336642.8:c.223A>T ENSP00000338009.4:p.Asn75Tyr
ENST00000345378.6:c.1174A>T ENSP00000223366.2:p.Asn392Tyr
ENST00000395796.7:c.1168A>T ENSP00000379142.3:p.Asn390Tyr
ENST00000403799.7:c.1171A>T ENSP00000384247.3:p.Asn391Tyr
ENST00000437084.1:c.1120A>T ENSP00000402840.1:p.Asn374Tyr
ENST00000459642.1:n.551A>T
ENST00000616242.4:c.1168A>T ENSP00000482149.1:p.Asn390Tyr
NM_000162.3:c.1171A>T NP_000153.1:p.Asn391Tyr
NM_033507.1:c.1174A>T NP_277042.1:p.Asn392Tyr
NM_033508.1:c.1168A>T NP_277043.1:p.Asn390Tyr
NM_000162.4:c.1171A>T NP_000153.1:p.Asn391Tyr
NM_001354800.1:c.1171A>T NP_001341729.1:p.Asn391Tyr
NM_001354801.1:c.160A>T NP_001341730.1:p.Asn54Tyr
NM_001354802.1:c.31A>T NP_001341731.1:p.Asn11Tyr
NM_001354803.1:c.205A>T NP_001341732.1:p.Asn69Tyr
NM_033507.2:c.1174A>T NP_277042.1:p.Asn392Tyr
NM_033508.2:c.1168A>T NP_277043.1:p.Asn390Tyr
XM_024446707.1:c.31A>T XP_024302475.1:p.Asn11Tyr
NM_000162.5:c.1171A>T MANE Select NP_000153.1:p.Asn391Tyr
NM_033507.3:c.1174A>T NP_277042.1:p.Asn392Tyr
NM_033508.3:c.1168A>T NP_277043.1:p.Asn390Tyr
NM_001354803.2:c.205A>T NP_001341732.1:p.Asn69Tyr