Canonical Allele Identifier: CA1703612948
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145669T= , CM000669.2:g.44145669T= GRCh38
NC_000007.13:g.44185268T= , CM000669.1:g.44185268T= GRCh37
NC_000007.12:g.44151793T= NCBI36
NG_008847.1:g.48755A=
NG_008847.2:g.57502A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1079A= ENSP00000379142.4:n.*1079A=
ENST00000616242.5:c.*201A= ENSP00000482149.2:n.*201A=
ENST00000683378.1:n.307A=
ENST00000336642.9:c.115A= ENSP00000338009.5:p.Thr39=
ENST00000345378.7:c.1084A= ENSP00000223366.2:p.Thr362=
ENST00000403799.8:c.1081A= MANE Select ENSP00000384247.3:p.Thr361=
ENST00000671824.1:c.1144A= ENSP00000500264.1:p.Thr382=
ENST00000672743.1:n.93A=
ENST00000673284.1:c.1081A= ENSP00000499852.1:p.Thr361=
ENST00000336642.8:c.133A= ENSP00000338009.4:p.Thr45=
ENST00000345378.6:c.1084A= ENSP00000223366.2:p.Thr362=
ENST00000395796.7:c.1078A= ENSP00000379142.3:p.Thr360=
ENST00000403799.7:c.1081A= ENSP00000384247.3:p.Thr361=
ENST00000437084.1:c.1030A= ENSP00000402840.1:p.Thr344=
ENST00000459642.1:n.461A=
ENST00000473353.1:n.379A=
ENST00000616242.4:c.1078A= ENSP00000482149.1:p.Thr360=
NM_000162.3:c.1081A= NP_000153.1:p.Thr361=
NM_033507.1:c.1084A= NP_277042.1:p.Thr362=
NM_033508.1:c.1078A= NP_277043.1:p.Thr360=
NM_000162.4:c.1081A= NP_000153.1:p.Thr361=
NM_001354800.1:c.1081A= NP_001341729.1:p.Thr361=
NM_001354801.1:c.70A= NP_001341730.1:p.Thr24=
NM_001354802.1:c.-60A= NP_001341731.1:n.-60A=
NM_001354803.1:c.115A= NP_001341732.1:p.Thr39=
NM_033507.2:c.1084A= NP_277042.1:p.Thr362=
NM_033508.2:c.1078A= NP_277043.1:p.Thr360=
XM_024446707.1:c.-60A= XP_024302475.1:n.-60A=
NM_000162.5:c.1081A= MANE Select NP_000153.1:p.Thr361=
NM_033507.3:c.1084A= NP_277042.1:p.Thr362=
NM_033508.3:c.1078A= NP_277043.1:p.Thr360=
NM_001354803.2:c.115A= NP_001341732.1:p.Thr39=