Canonical Allele Identifier: CA1703612909
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145602G= , CM000669.2:g.44145602G= GRCh38
NC_000007.13:g.44185201G= , CM000669.1:g.44185201G= GRCh37
NC_000007.12:g.44151726G= NCBI36
NG_008847.1:g.48822C=
NG_008847.2:g.57569C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1146C= ENSP00000379142.4:n.*1146C=
ENST00000616242.5:c.*268C= ENSP00000482149.2:n.*268C=
ENST00000683378.1:n.374C=
ENST00000336642.9:c.182C= ENSP00000338009.5:p.Ser61=
ENST00000345378.7:c.1151C= ENSP00000223366.2:p.Ser384=
ENST00000403799.8:c.1148C= MANE Select ENSP00000384247.3:p.Ser383=
ENST00000671824.1:c.1211C= ENSP00000500264.1:p.Ser404=
ENST00000672743.1:n.160C=
ENST00000673284.1:c.1148C= ENSP00000499852.1:p.Ser383=
ENST00000336642.8:c.200C= ENSP00000338009.4:p.Ser67=
ENST00000345378.6:c.1151C= ENSP00000223366.2:p.Ser384=
ENST00000395796.7:c.1145C= ENSP00000379142.3:p.Ser382=
ENST00000403799.7:c.1148C= ENSP00000384247.3:p.Ser383=
ENST00000437084.1:c.1097C= ENSP00000402840.1:p.Ser366=
ENST00000459642.1:n.528C=
ENST00000616242.4:c.1145C= ENSP00000482149.1:p.Ser382=
NM_000162.3:c.1148C= NP_000153.1:p.Ser383=
NM_033507.1:c.1151C= NP_277042.1:p.Ser384=
NM_033508.1:c.1145C= NP_277043.1:p.Ser382=
NM_000162.4:c.1148C= NP_000153.1:p.Ser383=
NM_001354800.1:c.1148C= NP_001341729.1:p.Ser383=
NM_001354801.1:c.137C= NP_001341730.1:p.Ser46=
NM_001354802.1:c.8C= NP_001341731.1:p.Ser3=
NM_001354803.1:c.182C= NP_001341732.1:p.Ser61=
NM_033507.2:c.1151C= NP_277042.1:p.Ser384=
NM_033508.2:c.1145C= NP_277043.1:p.Ser382=
XM_024446707.1:c.8C= XP_024302475.1:p.Ser3=
NM_000162.5:c.1148C= MANE Select NP_000153.1:p.Ser383=
NM_033507.3:c.1151C= NP_277042.1:p.Ser384=
NM_033508.3:c.1145C= NP_277043.1:p.Ser382=
NM_001354803.2:c.182C= NP_001341732.1:p.Ser61=