Canonical Allele Identifier: CA1703635868
Gene: GCK HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44149801_44149804delinsCAGG , CM000669.2:g.44149801_44149804delinsCAGG GRCh38
NC_000007.13:g.44189400_44189403delinsCAGG , CM000669.1:g.44189400_44189403delinsCAGG GRCh37
NC_000007.12:g.44155925_44155928delinsCAGG NCBI36
NG_008847.1:g.44620_44623delinsCCTG
NG_008847.2:g.53367_53370delinsCCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*633_*636delinsCCTG ENSP00000379142.4:n.*633_*636delinsCCTG
ENST00000616242.5:c.635_638delinsCCTG ENSP00000482149.2:p.Ser212=
ENST00000682635.1:n.1121_1124delinsCCTG
ENST00000345378.7:c.638_641delinsCCTG ENSP00000223366.2:p.Ser213=
ENST00000403799.8:c.635_638delinsCCTG MANE Select ENSP00000384247.3:p.Ser212=
ENST00000671824.1:c.635_638delinsCCTG ENSP00000500264.1:p.Ser212=
ENST00000673284.1:c.635_638delinsCCTG ENSP00000499852.1:p.Ser212=
ENST00000345378.6:c.638_641delinsCCTG ENSP00000223366.2:p.Ser213=
ENST00000395796.7:c.632_635delinsCCTG ENSP00000379142.3:p.Ser211=
ENST00000403799.7:c.635_638delinsCCTG ENSP00000384247.3:p.Ser212=
ENST00000437084.1:c.584_587delinsCCTG ENSP00000402840.1:p.Ser195=
ENST00000616242.4:c.632_635delinsCCTG ENSP00000482149.1:p.Ser211=
NM_000162.3:c.635_638delinsCCTG NP_000153.1:p.Ser212=
NM_033507.1:c.638_641delinsCCTG NP_277042.1:p.Ser213=
NM_033508.1:c.632_635delinsCCTG NP_277043.1:p.Ser211=
NM_000162.4:c.635_638delinsCCTG NP_000153.1:p.Ser212=
NM_001354800.1:c.635_638delinsCCTG NP_001341729.1:p.Ser212=
NM_033507.2:c.638_641delinsCCTG NP_277042.1:p.Ser213=
NM_033508.2:c.632_635delinsCCTG NP_277043.1:p.Ser211=
NM_000162.5:c.635_638delinsCCTG MANE Select NP_000153.1:p.Ser212=
NM_033507.3:c.638_641delinsCCTG NP_277042.1:p.Ser213=
NM_033508.3:c.632_635delinsCCTG NP_277043.1:p.Ser211=
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