Canonical Allele Identifier: CA1703636083
Gene: GCK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.44150210_44150229delinsGAGAGGTTTTGGGAACGATT , CM000669.2:g.44150210_44150229delinsGAGAGGTTTTGGGAACGATT GRCh38
NC_000007.13:g.44189809_44189828delinsGAGAGGTTTTGGGAACGATT , CM000669.1:g.44189809_44189828delinsGAGAGGTTTTGGGAACGATT GRCh37
NC_000007.12:g.44156334_44156353delinsGAGAGGTTTTGGGAACGATT NCBI36
NG_008847.1:g.44195_44214delinsAATCGTTCCCAAAACCTCTC
NG_008847.2:g.52942_52961delinsAATCGTTCCCAAAACCTCTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000395796.8:c.*482-165_*482-146delinsAATCGTTCCCAAAACCTCTC ENSP00000379142.4:n.*482-165_*482-146delinsAATCGTTCCCAAAACCTC...
ENST00000616242.5:c.484-165_484-146delinsAATCGTTCCCAAAACCTCTC ENSP00000482149.2:n.484-165_484-146delinsAATCGTTCCCAAAACCTCTC...
ENST00000682635.1:n.970-165_970-146delinsAATCGTTCCCAAAACCTCTC
ENST00000345378.7:c.487-165_487-146delinsAATCGTTCCCAAAACCTCTC ENSP00000223366.2:n.487-165_487-146delinsAATCGTTCCCAAAACCTCTC...
ENST00000403799.8:c.484-165_484-146delinsAATCGTTCCCAAAACCTCTC MANE Select ENSP00000384247.3:n.484-165_484-146delinsAATCGTTCCCAAAACCTCTC...
ENST00000671824.1:c.484-165_484-146delinsAATCGTTCCCAAAACCTCTC ENSP00000500264.1:n.484-165_484-146delinsAATCGTTCCCAAAACCTCTC...
ENST00000673284.1:c.484-165_484-146delinsAATCGTTCCCAAAACCTCTC ENSP00000499852.1:n.484-165_484-146delinsAATCGTTCCCAAAACCTCTC...
ENST00000345378.6:c.487-165_487-146delinsAATCGTTCCCAAAACCTCTC ENSP00000223366.2:n.487-165_487-146delinsAATCGTTCCCAAAACCTCTC...
ENST00000395796.7:c.481-165_481-146delinsAATCGTTCCCAAAACCTCTC ENSP00000379142.3:n.481-165_481-146delinsAATCGTTCCCAAAACCTCTC...
ENST00000403799.7:c.484-165_484-146delinsAATCGTTCCCAAAACCTCTC ENSP00000384247.3:n.484-165_484-146delinsAATCGTTCCCAAAACCTCTC...
ENST00000437084.1:c.433-165_433-146delinsAATCGTTCCCAAAACCTCTC ENSP00000402840.1:n.433-165_433-146delinsAATCGTTCCCAAAACCTCTC...
ENST00000616242.4:c.481-165_481-146delinsAATCGTTCCCAAAACCTCTC ENSP00000482149.1:n.481-165_481-146delinsAATCGTTCCCAAAACCTCTC...
NM_000162.3:c.484-165_484-146delinsAATCGTTCCCAAAACCTCTC NP_000153.1:n.484-165_484-146delinsAATCGTTCCCAAAACCTCTC
NM_033507.1:c.487-165_487-146delinsAATCGTTCCCAAAACCTCTC NP_277042.1:n.487-165_487-146delinsAATCGTTCCCAAAACCTCTC
NM_033508.1:c.481-165_481-146delinsAATCGTTCCCAAAACCTCTC NP_277043.1:n.481-165_481-146delinsAATCGTTCCCAAAACCTCTC
NM_000162.4:c.484-165_484-146delinsAATCGTTCCCAAAACCTCTC NP_000153.1:n.484-165_484-146delinsAATCGTTCCCAAAACCTCTC
NM_001354800.1:c.484-165_484-146delinsAATCGTTCCCAAAACCTCTC NP_001341729.1:n.484-165_484-146delinsAATCGTTCCCAAAACCTCTC
NM_033507.2:c.487-165_487-146delinsAATCGTTCCCAAAACCTCTC NP_277042.1:n.487-165_487-146delinsAATCGTTCCCAAAACCTCTC
NM_033508.2:c.481-165_481-146delinsAATCGTTCCCAAAACCTCTC NP_277043.1:n.481-165_481-146delinsAATCGTTCCCAAAACCTCTC
NM_000162.5:c.484-165_484-146delinsAATCGTTCCCAAAACCTCTC MANE Select NP_000153.1:n.484-165_484-146delinsAATCGTTCCCAAAACCTCTC
NM_033507.3:c.487-165_487-146delinsAATCGTTCCCAAAACCTCTC NP_277042.1:n.487-165_487-146delinsAATCGTTCCCAAAACCTCTC
NM_033508.3:c.481-165_481-146delinsAATCGTTCCCAAAACCTCTC NP_277043.1:n.481-165_481-146delinsAATCGTTCCCAAAACCTCTC