Canonical Allele Identifier: CA1703612684
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145225T= , CM000669.2:g.44145225T= GRCh38
NC_000007.13:g.44184824T= , CM000669.1:g.44184824T= GRCh37
NC_000007.12:g.44151349T= NCBI36
NG_008847.1:g.49199A=
NG_008847.2:g.57946A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1307A= ENSP00000379142.4:n.*1307A=
ENST00000616242.5:c.*429A= ENSP00000482149.2:n.*429A=
ENST00000683378.1:n.535A=
ENST00000336642.9:c.343A= ENSP00000338009.5:p.Thr115=
ENST00000345378.7:c.1312A= ENSP00000223366.2:p.Thr438=
ENST00000403799.8:c.1309A= MANE Select ENSP00000384247.3:p.Thr437=
ENST00000671824.1:c.1372A= ENSP00000500264.1:p.Thr458=
ENST00000672743.1:n.321A=
ENST00000673284.1:c.1309A= ENSP00000499852.1:p.Thr437=
ENST00000336642.8:c.361A= ENSP00000338009.4:p.Thr121=
ENST00000345378.6:c.1312A= ENSP00000223366.2:p.Thr438=
ENST00000395796.7:c.1306A= ENSP00000379142.3:p.Thr436=
ENST00000403799.7:c.1309A= ENSP00000384247.3:p.Thr437=
ENST00000437084.1:c.1258A= ENSP00000402840.1:p.Thr420=
ENST00000459642.1:n.689A=
ENST00000616242.4:c.1306A= ENSP00000482149.1:p.Thr436=
NM_000162.3:c.1309A= NP_000153.1:p.Thr437=
NM_033507.1:c.1312A= NP_277042.1:p.Thr438=
NM_033508.1:c.1306A= NP_277043.1:p.Thr436=
NM_000162.4:c.1309A= NP_000153.1:p.Thr437=
NM_001354800.1:c.1309A= NP_001341729.1:p.Thr437=
NM_001354801.1:c.298A= NP_001341730.1:p.Thr100=
NM_001354802.1:c.169A= NP_001341731.1:p.Thr57=
NM_001354803.1:c.343A= NP_001341732.1:p.Thr115=
NM_033507.2:c.1312A= NP_277042.1:p.Thr438=
NM_033508.2:c.1306A= NP_277043.1:p.Thr436=
XM_024446707.1:c.169A= XP_024302475.1:p.Thr57=
NM_000162.5:c.1309A= MANE Select NP_000153.1:p.Thr437=
NM_033507.3:c.1312A= NP_277042.1:p.Thr438=
NM_033508.3:c.1306A= NP_277043.1:p.Thr436=
NM_001354803.2:c.343A= NP_001341732.1:p.Thr115=