Canonical Allele Identifier: CA1703612821
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145472C= , CM000669.2:g.44145472C= GRCh38
NC_000007.13:g.44185071C= , CM000669.1:g.44185071C= GRCh37
NC_000007.12:g.44151596C= NCBI36
NG_008847.1:g.48952G=
NG_008847.2:g.57699G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1251+25G= ENSP00000379142.4:n.*1251+25G=
ENST00000616242.5:c.*373+25G= ENSP00000482149.2:n.*373+25G=
ENST00000683378.1:n.479+25G=
ENST00000336642.9:c.287+25G= ENSP00000338009.5:n.287+25G=
ENST00000345378.7:c.1256+25G= ENSP00000223366.2:n.1256+25G=
ENST00000403799.8:c.1253+25G= MANE Select ENSP00000384247.3:n.1253+25G=
ENST00000671824.1:c.1316+25G= ENSP00000500264.1:n.1316+25G=
ENST00000672743.1:n.265+25G=
ENST00000673284.1:c.1253+25G= ENSP00000499852.1:n.1253+25G=
ENST00000336642.8:c.305+25G= ENSP00000338009.4:n.305+25G=
ENST00000345378.6:c.1256+25G= ENSP00000223366.2:n.1256+25G=
ENST00000395796.7:c.1250+25G= ENSP00000379142.3:n.1250+25G=
ENST00000403799.7:c.1253+25G= ENSP00000384247.3:n.1253+25G=
ENST00000437084.1:c.1202+25G= ENSP00000402840.1:n.1202+25G=
ENST00000459642.1:n.633+25G=
ENST00000616242.4:c.1250+25G= ENSP00000482149.1:n.1250+25G=
NM_000162.3:c.1253+25G= NP_000153.1:n.1253+25G=
NM_033507.1:c.1256+25G= NP_277042.1:n.1256+25G=
NM_033508.1:c.1250+25G= NP_277043.1:n.1250+25G=
NM_000162.4:c.1253+25G= NP_000153.1:n.1253+25G=
NM_001354800.1:c.1253+25G= NP_001341729.1:n.1253+25G=
NM_001354801.1:c.242+25G= NP_001341730.1:n.242+25G=
NM_001354802.1:c.113+25G= NP_001341731.1:n.113+25G=
NM_001354803.1:c.287+25G= NP_001341732.1:n.287+25G=
NM_033507.2:c.1256+25G= NP_277042.1:n.1256+25G=
NM_033508.2:c.1250+25G= NP_277043.1:n.1250+25G=
XM_024446707.1:c.113+25G= XP_024302475.1:n.113+25G=
NM_000162.5:c.1253+25G= MANE Select NP_000153.1:n.1253+25G=
NM_033507.3:c.1256+25G= NP_277042.1:n.1256+25G=
NM_033508.3:c.1250+25G= NP_277043.1:n.1250+25G=
NM_001354803.2:c.287+25G= NP_001341732.1:n.287+25G=