Canonical Allele Identifier: CA2682576761
Gene: GCK HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44153430_44153432del , CM000669.2:g.44153430_44153432del GRCh38
NC_000007.13:g.44193029_44193031del , CM000669.1:g.44193029_44193031del GRCh37
NC_000007.12:g.44159554_44159556del NCBI36
NG_008847.1:g.40999_41001del
NG_008847.2:g.49746_49748del

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*82_*84del ENSP00000379142.4:n.*82_*84del
ENST00000616242.5:c.84_86del ENSP00000482149.2:p.Glu28del
ENST00000682635.1:n.570_572del
ENST00000345378.7:c.87_89del ENSP00000223366.2:p.Glu29del
ENST00000403799.8:c.84_86del MANE Select ENSP00000384247.3:p.Glu28del
ENST00000671824.1:c.84_86del ENSP00000500264.1:p.Glu28del
ENST00000673284.1:c.84_86del ENSP00000499852.1:p.Glu28del
ENST00000345378.6:c.87_89del ENSP00000223366.2:p.Glu29del
ENST00000395796.7:c.81_83del ENSP00000379142.3:p.Glu27del
ENST00000403799.7:c.84_86del ENSP00000384247.3:p.Glu28del
ENST00000437084.1:c.84_86del ENSP00000402840.1:p.Glu28del
ENST00000476008.1:n.519_521del
ENST00000616242.4:c.81_83del ENSP00000482149.1:p.Glu27del
NM_000162.3:c.84_86del NP_000153.1:p.Glu28del
NM_033507.1:c.87_89del NP_277042.1:p.Glu29del
NM_033508.1:c.81_83del NP_277043.1:p.Glu27del
NM_000162.4:c.84_86del NP_000153.1:p.Glu28del
NM_001354800.1:c.84_86del NP_001341729.1:p.Glu28del
NM_033507.2:c.87_89del NP_277042.1:p.Glu29del
NM_033508.2:c.81_83del NP_277043.1:p.Glu27del
NM_000162.5:c.84_86del MANE Select NP_000153.1:p.Glu28del
NM_033507.3:c.87_89del NP_277042.1:p.Glu29del
NM_033508.3:c.81_83del NP_277043.1:p.Glu27del