Canonical Allele Identifier: CA2756266615
Gene: GLYCTK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.52292633_52292634insA , CM000665.2:g.52292633_52292634insA GRCh38
NC_000003.11:g.52326649_52326650insA , CM000665.1:g.52326649_52326650insA GRCh37
NC_000003.10:g.52301689_52301690insA NCBI36
NG_023246.1:g.9814_9815insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000436784.7:c.1079_1080insA MANE Select ENSP00000389175.2:p.Ser362IlefsTer15
ENST00000305690.12:c.*198_*199insA ENSP00000301965.9:n.*198_*199insA
ENST00000436784.6:c.1079_1080insA ENSP00000389175.2:p.Ser362IlefsTer15
ENST00000461183.5:c.763+64_763+65insA ENSP00000417264.1:n.763+64_763+65insA
ENST00000471180.5:c.634+64_634+65insA ENSP00000417526.1:n.634+64_634+65insA
ENST00000473032.5:c.530-413_530-412insA ENSP00000418951.1:n.530-413_530-412insA
ENST00000477382.1:c.*198_*199insA ENSP00000419008.1:n.*198_*199insA
ENST00000486393.5:c.*442_*443insA ENSP00000419868.1:n.*442_*443insA
ENST00000489173.1:n.1373_1374insA
NM_001144951.1:c.*198_*199insA NP_001138423.1:n.*198_*199insA
NM_145262.3:c.1079_1080insA NP_660305.2:p.Ser362IlefsTer15
NR_026699.1:n.1177_1178insA
NR_026700.1:n.695+64_695+65insA
NR_026701.1:n.1175_1176insA
NR_026702.1:n.626-413_626-412insA
XM_005264878.2:c.*198_*199insA XP_005264935.1:n.*198_*199insA
XR_245095.2:n.2742+64_2742+65insA
XM_017005730.1:c.698_699insA XP_016861219.1:p.Ser235IlefsTer15
XM_024453351.1:c.1079_1080insA XP_024309119.1:p.Ser362IlefsTer15
XM_024453352.1:c.*198_*199insA XP_024309120.1:n.*198_*199insA
XR_001740022.2:n.2981_2982insA
XR_001740023.2:n.2917+64_2917+65insA
XR_245095.4:n.2743+64_2743+65insA
NM_145262.4:c.1079_1080insA MANE Select NP_660305.2:p.Ser362IlefsTer15
NR_026699.2:n.1169_1170insA
NR_026700.2:n.687+64_687+65insA
NR_026701.2:n.1167_1168insA
NR_026702.2:n.618-413_618-412insA
NM_001144951.2:c.*198_*199insA NP_001138423.1:n.*198_*199insA