Canonical Allele Identifier: CA2695202952
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44150958_44150960dup , CM000669.2:g.44150958_44150960dup GRCh38
NC_000007.13:g.44190557_44190559dup , CM000669.1:g.44190557_44190559dup GRCh37
NC_000007.12:g.44157082_44157084dup NCBI36
NG_008847.1:g.43465_43467dup
NG_008847.2:g.52212_52214dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*478_*480dup ENSP00000379142.4:n.*478_*480dup
ENST00000616242.5:c.480_482dup ENSP00000482149.2:p.Asp160_Lys161insAsn
ENST00000682635.1:n.966_968dup
ENST00000345378.7:c.483_485dup ENSP00000223366.2:p.Asp161_Lys162insAsn
ENST00000403799.8:c.480_482dup MANE Select ENSP00000384247.3:p.Asp160_Lys161insAsn
ENST00000671824.1:c.480_482dup ENSP00000500264.1:p.Asp160_Lys161insAsn
ENST00000673284.1:c.480_482dup ENSP00000499852.1:p.Asp160_Lys161insAsn
ENST00000345378.6:c.483_485dup ENSP00000223366.2:p.Asp161_Lys162insAsn
ENST00000395796.7:c.477_479dup ENSP00000379142.3:p.Asp159_Lys160insAsn
ENST00000403799.7:c.480_482dup ENSP00000384247.3:p.Asp160_Lys161insAsn
ENST00000437084.1:c.429_431dup ENSP00000402840.1:p.Asp143_Lys144insAsn
ENST00000616242.4:c.477_479dup ENSP00000482149.1:p.Asp159_Lys160insAsn
NM_000162.3:c.480_482dup NP_000153.1:p.Asp160_Lys161insAsn
NM_033507.1:c.483_485dup NP_277042.1:p.Asp161_Lys162insAsn
NM_033508.1:c.477_479dup NP_277043.1:p.Asp159_Lys160insAsn
NM_000162.4:c.480_482dup NP_000153.1:p.Asp160_Lys161insAsn
NM_001354800.1:c.480_482dup NP_001341729.1:p.Asp160_Lys161insAsn
NM_033507.2:c.483_485dup NP_277042.1:p.Asp161_Lys162insAsn
NM_033508.2:c.477_479dup NP_277043.1:p.Asp159_Lys160insAsn
NM_000162.5:c.480_482dup MANE Select NP_000153.1:p.Asp160_Lys161insAsn
NM_033507.3:c.483_485dup NP_277042.1:p.Asp161_Lys162insAsn
NM_033508.3:c.477_479dup NP_277043.1:p.Asp159_Lys160insAsn