Canonical Allele Identifier: CA1364789024
Gene: GLYCTK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52292608_52292609delinsGC , CM000665.2:g.52292608_52292609delinsGC GRCh38
NC_000003.11:g.52326624_52326625delinsGC , CM000665.1:g.52326624_52326625delinsGC GRCh37
NC_000003.10:g.52301664_52301665delinsGC NCBI36
NG_023246.1:g.9789_9790delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000436784.7:c.1054_1055delinsGC MANE Select ENSP00000389175.2:p.Ala352=
ENST00000305690.12:c.*173_*174delinsGC ENSP00000301965.9:n.*173_*174delinsGC
ENST00000436784.6:c.1054_1055delinsGC ENSP00000389175.2:p.Ala352=
ENST00000461183.5:c.763+39_763+40delinsGC ENSP00000417264.1:n.763+39_763+40delinsGC
ENST00000471180.5:c.634+39_634+40delinsGC ENSP00000417526.1:n.634+39_634+40delinsGC
ENST00000473032.5:c.530-438_530-437delinsGC ENSP00000418951.1:n.530-438_530-437delinsGC
ENST00000477382.1:c.*173_*174delinsGC ENSP00000419008.1:n.*173_*174delinsGC
ENST00000486393.5:c.*417_*418delinsGC ENSP00000419868.1:n.*417_*418delinsGC
ENST00000489173.1:n.1348_1349delinsGC
NM_001144951.1:c.*173_*174delinsGC NP_001138423.1:n.*173_*174delinsGC
NM_145262.3:c.1054_1055delinsGC NP_660305.2:p.Ala352=
NR_026699.1:n.1152_1153delinsGC
NR_026700.1:n.695+39_695+40delinsGC
NR_026701.1:n.1150_1151delinsGC
NR_026702.1:n.626-438_626-437delinsGC
XM_005264878.2:c.*173_*174delinsGC XP_005264935.1:n.*173_*174delinsGC
XR_245095.2:n.2742+39_2742+40delinsGC
XM_017005730.1:c.673_674delinsGC XP_016861219.1:p.Ala225=
XM_024453351.1:c.1054_1055delinsGC XP_024309119.1:p.Ala352=
XM_024453352.1:c.*173_*174delinsGC XP_024309120.1:n.*173_*174delinsGC
XR_001740022.2:n.2956_2957delinsGC
XR_001740023.2:n.2917+39_2917+40delinsGC
XR_245095.4:n.2743+39_2743+40delinsGC
NM_145262.4:c.1054_1055delinsGC MANE Select NP_660305.2:p.Ala352=
NR_026699.2:n.1144_1145delinsGC
NR_026700.2:n.687+39_687+40delinsGC
NR_026701.2:n.1142_1143delinsGC
NR_026702.2:n.618-438_618-437delinsGC
NM_001144951.2:c.*173_*174delinsGC NP_001138423.1:n.*173_*174delinsGC