Canonical Allele Identifier: CA2577780409
Gene: GLYCTK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52292686_52292697del , CM000665.2:g.52292686_52292697del GRCh38
NC_000003.11:g.52326702_52326713del , CM000665.1:g.52326702_52326713del GRCh37
NC_000003.10:g.52301742_52301753del NCBI36
NG_023246.1:g.9867_9878del

Transcript Alleles

HGVS Amino-acid Change
ENST00000436784.7:c.1132_1143del MANE Select ENSP00000389175.2:p.Ala378_Leu381del
ENST00000305690.12:c.*251_*262del ENSP00000301965.9:n.*251_*262del
ENST00000436784.6:c.1132_1143del ENSP00000389175.2:p.Ala378_Leu381del
ENST00000461183.5:c.763+117_763+128del ENSP00000417264.1:n.763+117_763+128del
ENST00000471180.5:c.634+117_634+128del ENSP00000417526.1:n.634+117_634+128del
ENST00000473032.5:c.530-360_530-349del ENSP00000418951.1:n.530-360_530-349del
ENST00000477382.1:c.*251_*262del ENSP00000419008.1:n.*251_*262del
ENST00000486393.5:c.*495_*506del ENSP00000419868.1:n.*495_*506del
ENST00000489173.1:n.1426_1437del
NM_001144951.1:c.*251_*262del NP_001138423.1:n.*251_*262del
NM_145262.3:c.1132_1143del NP_660305.2:p.Ala378_Leu381del
NR_026699.1:n.1230_1241del
NR_026700.1:n.695+117_695+128del
NR_026701.1:n.1228_1239del
NR_026702.1:n.626-360_626-349del
XM_005264878.2:c.*251_*262del XP_005264935.1:n.*251_*262del
XR_245095.2:n.2742+117_2742+128del
XM_017005730.1:c.751_762del XP_016861219.1:p.Ala251_Leu254del
XM_024453351.1:c.1132_1143del XP_024309119.1:p.Ala378_Leu381del
XM_024453352.1:c.*251_*262del XP_024309120.1:n.*251_*262del
XR_001740022.2:n.3034_3045del
XR_001740023.2:n.2917+117_2917+128del
XR_245095.4:n.2743+117_2743+128del
NM_145262.4:c.1132_1143del MANE Select NP_660305.2:p.Ala378_Leu381del
NR_026699.2:n.1222_1233del
NR_026700.2:n.687+117_687+128del
NR_026701.2:n.1220_1231del
NR_026702.2:n.618-360_618-349del
NM_001144951.2:c.*251_*262del NP_001138423.1:n.*251_*262del