Canonical Allele Identifier: CA2631709371
Gene: CIITA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.10877129_10877146del , CM000678.2:g.10877129_10877146del GRCh38
NC_000016.9:g.10970986_10971003del , CM000678.1:g.10970986_10971003del GRCh37
NC_000016.8:g.10878487_10878504del NCBI36
NG_009628.1:g.4932_4949del , LRG_49:g.4932_4949del

Transcript Alleles

HGVS Amino-acid Change
ENST00000636238.1:c.-21+10810_-21+10827del ENSP00000490205.1:n.-21+10810_-21+10827del
ENST00000637439.1:c.283+10557_283+10574del ENSP00000489907.1:n.283+10557_283+10574del
XM_006720880.2:c.346+10557_346+10574del XP_006720943.2:n.346+10557_346+10574del
XM_011522484.1:c.346+10557_346+10574del XP_011520786.1:n.346+10557_346+10574del
XM_011522485.1:c.346+10557_346+10574del XP_011520787.1:n.346+10557_346+10574del
XM_011522486.1:c.346+10557_346+10574del XP_011520788.1:n.346+10557_346+10574del
XM_011522487.1:c.247+10557_247+10574del XP_011520789.1:n.247+10557_247+10574del
XM_011522489.1:c.247+10557_247+10574del XP_011520791.1:n.247+10557_247+10574del
XM_011522491.1:c.346+10557_346+10574del XP_011520793.1:n.346+10557_346+10574del
XM_011522494.1:c.-21+10810_-21+10827del XP_011520796.1:n.-21+10810_-21+10827del
XR_932841.1:n.361+10557_361+10574del
XR_932842.1:n.361+10557_361+10574del
XR_932843.1:n.361+10557_361+10574del
XR_932846.1:n.361+10557_361+10574del
XR_932847.1:n.361+10557_361+10574del
XR_933067.1:n.1162+11169_1162+11186del
XR_933068.1:n.1162+11169_1162+11186del
XM_006720880.3:c.346+10557_346+10574del XP_006720943.2:n.346+10557_346+10574del
XM_011522484.3:c.346+10557_346+10574del XP_011520786.1:n.346+10557_346+10574del
XM_011522485.2:c.346+10557_346+10574del XP_011520787.1:n.346+10557_346+10574del
XM_011522486.2:c.346+10557_346+10574del XP_011520788.1:n.346+10557_346+10574del
XM_011522487.2:c.247+10557_247+10574del XP_011520789.1:n.247+10557_247+10574del
XM_011522489.2:c.247+10557_247+10574del XP_011520791.1:n.247+10557_247+10574del
XM_011522491.2:c.346+10557_346+10574del XP_011520793.1:n.346+10557_346+10574del
XM_011522492.2:c.-202_-185del XP_011520794.1:n.-202_-185del
XM_011522493.2:c.-202_-185del XP_011520795.1:n.-202_-185del
XM_011522494.2:c.-21+10810_-21+10827del XP_011520796.1:n.-21+10810_-21+10827del
XM_011522495.2:c.-202_-185del XP_011520797.1:n.-202_-185del
XM_011522496.2:c.-202_-185del XP_011520798.1:n.-202_-185del
XM_024450280.1:c.-202_-185del XP_024306048.1:n.-202_-185del
XM_024450281.1:c.-202_-185del XP_024306049.1:n.-202_-185del
XR_001751904.1:n.365+10557_365+10574del
XR_002957860.1:n.1246+11169_1246+11186del
XR_002957861.1:n.1246+11169_1246+11186del
XR_002957863.1:n.1442+5873_1442+5890del
XR_932841.3:n.363+10557_363+10574del
XR_932842.2:n.363+10557_363+10574del
XR_932846.3:n.365+10557_365+10574del
XR_932847.3:n.365+10557_365+10574del