Canonical Allele Identifier: CA2631709324
Gene: CIITA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.10877077_10877078del , CM000678.2:g.10877077_10877078del GRCh38
NC_000016.9:g.10970934_10970935del , CM000678.1:g.10970934_10970935del GRCh37
NC_000016.8:g.10878435_10878436del NCBI36
NG_009628.1:g.4880_4881del , LRG_49:g.4880_4881del

Transcript Alleles

HGVS Amino-acid change
ENST00000636238.1:c.-21+10758_-21+10759del ENSP00000490205.1:n.-21+10758_-21+10759de...
ENST00000637439.1:c.283+10505_283+10506del ENSP00000489907.1:n.283+10505_283+10506de...
XM_006720880.2:c.346+10505_346+10506del XP_006720943.2:n.346+10505_346+10506del
XM_011522484.1:c.346+10505_346+10506del XP_011520786.1:n.346+10505_346+10506del
XM_011522485.1:c.346+10505_346+10506del XP_011520787.1:n.346+10505_346+10506del
XM_011522486.1:c.346+10505_346+10506del XP_011520788.1:n.346+10505_346+10506del
XM_011522487.1:c.247+10505_247+10506del XP_011520789.1:n.247+10505_247+10506del
XM_011522489.1:c.247+10505_247+10506del XP_011520791.1:n.247+10505_247+10506del
XM_011522491.1:c.346+10505_346+10506del XP_011520793.1:n.346+10505_346+10506del
XM_011522494.1:c.-21+10758_-21+10759del XP_011520796.1:n.-21+10758_-21+10759del
XR_932841.1:n.361+10505_361+10506del
XR_932842.1:n.361+10505_361+10506del
XR_932843.1:n.361+10505_361+10506del
XR_932846.1:n.361+10505_361+10506del
XR_932847.1:n.361+10505_361+10506del
XR_933067.1:n.1162+11239_1162+11240del
XR_933068.1:n.1162+11239_1162+11240del
XM_006720880.3:c.346+10505_346+10506del XP_006720943.2:n.346+10505_346+10506del
XM_011522484.3:c.346+10505_346+10506del XP_011520786.1:n.346+10505_346+10506del
XM_011522485.2:c.346+10505_346+10506del XP_011520787.1:n.346+10505_346+10506del
XM_011522486.2:c.346+10505_346+10506del XP_011520788.1:n.346+10505_346+10506del
XM_011522487.2:c.247+10505_247+10506del XP_011520789.1:n.247+10505_247+10506del
XM_011522489.2:c.247+10505_247+10506del XP_011520791.1:n.247+10505_247+10506del
XM_011522491.2:c.346+10505_346+10506del XP_011520793.1:n.346+10505_346+10506del
XM_011522492.2:c.-254_-253del XP_011520794.1:n.-254_-253del
XM_011522493.2:c.-254_-253del XP_011520795.1:n.-254_-253del
XM_011522494.2:c.-21+10758_-21+10759del XP_011520796.1:n.-21+10758_-21+10759del
XM_011522495.2:c.-254_-253del XP_011520797.1:n.-254_-253del
XM_011522496.2:c.-254_-253del XP_011520798.1:n.-254_-253del
XM_024450280.1:c.-254_-253del XP_024306048.1:n.-254_-253del
XM_024450281.1:c.-254_-253del XP_024306049.1:n.-254_-253del
XR_001751904.1:n.365+10505_365+10506del
XR_002957860.1:n.1246+11239_1246+11240del
XR_002957861.1:n.1246+11239_1246+11240del
XR_002957863.1:n.1442+5943_1442+5944del
XR_932841.3:n.363+10505_363+10506del
XR_932842.2:n.363+10505_363+10506del
XR_932846.3:n.365+10505_365+10506del
XR_932847.3:n.365+10505_365+10506del