Canonical Allele Identifier: CA1703612899
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44145594G= , CM000669.2:g.44145594G= GRCh38
NC_000007.13:g.44185193G= , CM000669.1:g.44185193G= GRCh37
NC_000007.12:g.44151718G= NCBI36
NG_008847.1:g.48830C=
NG_008847.2:g.57577C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*1154C= ENSP00000379142.4:n.*1154C=
ENST00000616242.5:c.*276C= ENSP00000482149.2:n.*276C=
ENST00000683378.1:n.382C=
ENST00000336642.9:c.190C= ENSP00000338009.5:p.Leu64=
ENST00000345378.7:c.1159C= ENSP00000223366.2:p.Leu387=
ENST00000403799.8:c.1156C= MANE Select ENSP00000384247.3:p.Leu386=
ENST00000671824.1:c.1219C= ENSP00000500264.1:p.Leu407=
ENST00000672743.1:n.168C=
ENST00000673284.1:c.1156C= ENSP00000499852.1:p.Leu386=
ENST00000336642.8:c.208C= ENSP00000338009.4:p.Leu70=
ENST00000345378.6:c.1159C= ENSP00000223366.2:p.Leu387=
ENST00000395796.7:c.1153C= ENSP00000379142.3:p.Leu385=
ENST00000403799.7:c.1156C= ENSP00000384247.3:p.Leu386=
ENST00000437084.1:c.1105C= ENSP00000402840.1:p.Leu369=
ENST00000459642.1:n.536C=
ENST00000616242.4:c.1153C= ENSP00000482149.1:p.Leu385=
NM_000162.3:c.1156C= NP_000153.1:p.Leu386=
NM_033507.1:c.1159C= NP_277042.1:p.Leu387=
NM_033508.1:c.1153C= NP_277043.1:p.Leu385=
NM_000162.4:c.1156C= NP_000153.1:p.Leu386=
NM_001354800.1:c.1156C= NP_001341729.1:p.Leu386=
NM_001354801.1:c.145C= NP_001341730.1:p.Leu49=
NM_001354802.1:c.16C= NP_001341731.1:p.Leu6=
NM_001354803.1:c.190C= NP_001341732.1:p.Leu64=
NM_033507.2:c.1159C= NP_277042.1:p.Leu387=
NM_033508.2:c.1153C= NP_277043.1:p.Leu385=
XM_024446707.1:c.16C= XP_024302475.1:p.Leu6=
NM_000162.5:c.1156C= MANE Select NP_000153.1:p.Leu386=
NM_033507.3:c.1159C= NP_277042.1:p.Leu387=
NM_033508.3:c.1153C= NP_277043.1:p.Leu385=
NM_001354803.2:c.190C= NP_001341732.1:p.Leu64=