Canonical Allele Identifier: CA2207312907
Gene: CIITA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.10877101_10877102delinsAC , CM000678.2:g.10877101_10877102delinsAC GRCh38
NC_000016.9:g.10970958_10970959delinsAC , CM000678.1:g.10970958_10970959delinsAC GRCh37
NC_000016.8:g.10878459_10878460delinsAC NCBI36
NG_009628.1:g.4904_4905delinsAC , LRG_49:g.4904_4905delinsAC

Transcript Alleles

HGVS Amino-acid change
ENST00000636238.1:c.-21+10782_-21+10783delinsAC ENSP00000490205.1:n.-21+10782_-21+10783delinsAC
ENST00000637439.1:c.283+10529_283+10530delinsAC ENSP00000489907.1:n.283+10529_283+10530delinsAC
XM_006720880.2:c.346+10529_346+10530delinsAC XP_006720943.2:n.346+10529_346+10530delinsAC
XM_011522484.1:c.346+10529_346+10530delinsAC XP_011520786.1:n.346+10529_346+10530delinsAC
XM_011522485.1:c.346+10529_346+10530delinsAC XP_011520787.1:n.346+10529_346+10530delinsAC
XM_011522486.1:c.346+10529_346+10530delinsAC XP_011520788.1:n.346+10529_346+10530delinsAC
XM_011522487.1:c.247+10529_247+10530delinsAC XP_011520789.1:n.247+10529_247+10530delinsAC
XM_011522489.1:c.247+10529_247+10530delinsAC XP_011520791.1:n.247+10529_247+10530delinsAC
XM_011522491.1:c.346+10529_346+10530delinsAC XP_011520793.1:n.346+10529_346+10530delinsAC
XM_011522494.1:c.-21+10782_-21+10783delinsAC XP_011520796.1:n.-21+10782_-21+10783delinsAC
XR_932841.1:n.361+10529_361+10530delinsAC
XR_932842.1:n.361+10529_361+10530delinsAC
XR_932843.1:n.361+10529_361+10530delinsAC
XR_932846.1:n.361+10529_361+10530delinsAC
XR_932847.1:n.361+10529_361+10530delinsAC
XR_933067.1:n.1162+11213_1162+11214delinsGT
XR_933068.1:n.1162+11213_1162+11214delinsGT
XM_006720880.3:c.346+10529_346+10530delinsAC XP_006720943.2:n.346+10529_346+10530delinsAC
XM_011522484.3:c.346+10529_346+10530delinsAC XP_011520786.1:n.346+10529_346+10530delinsAC
XM_011522485.2:c.346+10529_346+10530delinsAC XP_011520787.1:n.346+10529_346+10530delinsAC
XM_011522486.2:c.346+10529_346+10530delinsAC XP_011520788.1:n.346+10529_346+10530delinsAC
XM_011522487.2:c.247+10529_247+10530delinsAC XP_011520789.1:n.247+10529_247+10530delinsAC
XM_011522489.2:c.247+10529_247+10530delinsAC XP_011520791.1:n.247+10529_247+10530delinsAC
XM_011522491.2:c.346+10529_346+10530delinsAC XP_011520793.1:n.346+10529_346+10530delinsAC
XM_011522492.2:c.-230_-229delinsAC XP_011520794.1:n.-230_-229delinsAC
XM_011522493.2:c.-230_-229delinsAC XP_011520795.1:n.-230_-229delinsAC
XM_011522494.2:c.-21+10782_-21+10783delinsAC XP_011520796.1:n.-21+10782_-21+10783delinsAC
XM_011522495.2:c.-230_-229delinsAC XP_011520797.1:n.-230_-229delinsAC
XM_011522496.2:c.-230_-229delinsAC XP_011520798.1:n.-230_-229delinsAC
XM_024450280.1:c.-230_-229delinsAC XP_024306048.1:n.-230_-229delinsAC
XM_024450281.1:c.-230_-229delinsAC XP_024306049.1:n.-230_-229delinsAC
XR_001751904.1:n.365+10529_365+10530delinsAC
XR_002957860.1:n.1246+11213_1246+11214delinsGT
XR_002957861.1:n.1246+11213_1246+11214delinsGT
XR_002957863.1:n.1442+5917_1442+5918delinsGT
XR_932841.3:n.363+10529_363+10530delinsAC
XR_932842.2:n.363+10529_363+10530delinsAC
XR_932846.3:n.365+10529_365+10530delinsAC
XR_932847.3:n.365+10529_365+10530delinsAC