Canonical Allele Identifier: CA2207312930

Gene: CIITA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10877150_10877151delinsTG , CM000678.2:g.10877150_10877151delinsTG	GRCh38
NC_000016.9:g.10971007_10971008delinsTG , CM000678.1:g.10971007_10971008delinsTG	GRCh37
NC_000016.8:g.10878508_10878509delinsTG	NCBI36
NG_009628.1:g.4953_4954delinsTG , LRG_49:g.4953_4954delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000636238.1:c.-21+10831_-21+10832delinsTG	ENSP00000490205.1:n.-21+10831_-21+10832delinsTG
ENST00000637439.1:c.283+10578_283+10579delinsTG	ENSP00000489907.1:n.283+10578_283+10579delinsTG
XM_006720880.2:c.346+10578_346+10579delinsTG	XP_006720943.2:n.346+10578_346+10579delinsTG
XM_011522484.1:c.346+10578_346+10579delinsTG	XP_011520786.1:n.346+10578_346+10579delinsTG
XM_011522485.1:c.346+10578_346+10579delinsTG	XP_011520787.1:n.346+10578_346+10579delinsTG
XM_011522486.1:c.346+10578_346+10579delinsTG	XP_011520788.1:n.346+10578_346+10579delinsTG
XM_011522487.1:c.247+10578_247+10579delinsTG	XP_011520789.1:n.247+10578_247+10579delinsTG
XM_011522489.1:c.247+10578_247+10579delinsTG	XP_011520791.1:n.247+10578_247+10579delinsTG
XM_011522491.1:c.346+10578_346+10579delinsTG	XP_011520793.1:n.346+10578_346+10579delinsTG
XM_011522494.1:c.-21+10831_-21+10832delinsTG	XP_011520796.1:n.-21+10831_-21+10832delinsTG
XR_932841.1:n.361+10578_361+10579delinsTG
XR_932842.1:n.361+10578_361+10579delinsTG
XR_932843.1:n.361+10578_361+10579delinsTG
XR_932846.1:n.361+10578_361+10579delinsTG
XR_932847.1:n.361+10578_361+10579delinsTG
XR_933067.1:n.1162+11164_1162+11165delinsCA
XR_933068.1:n.1162+11164_1162+11165delinsCA
XM_006720880.3:c.346+10578_346+10579delinsTG	XP_006720943.2:n.346+10578_346+10579delinsTG
XM_011522484.3:c.346+10578_346+10579delinsTG	XP_011520786.1:n.346+10578_346+10579delinsTG
XM_011522485.2:c.346+10578_346+10579delinsTG	XP_011520787.1:n.346+10578_346+10579delinsTG
XM_011522486.2:c.346+10578_346+10579delinsTG	XP_011520788.1:n.346+10578_346+10579delinsTG
XM_011522487.2:c.247+10578_247+10579delinsTG	XP_011520789.1:n.247+10578_247+10579delinsTG
XM_011522489.2:c.247+10578_247+10579delinsTG	XP_011520791.1:n.247+10578_247+10579delinsTG
XM_011522491.2:c.346+10578_346+10579delinsTG	XP_011520793.1:n.346+10578_346+10579delinsTG
XM_011522492.2:c.-181_-180delinsTG	XP_011520794.1:n.-181_-180delinsTG
XM_011522493.2:c.-181_-180delinsTG	XP_011520795.1:n.-181_-180delinsTG
XM_011522494.2:c.-21+10831_-21+10832delinsTG	XP_011520796.1:n.-21+10831_-21+10832delinsTG
XM_011522495.2:c.-181_-180delinsTG	XP_011520797.1:n.-181_-180delinsTG
XM_011522496.2:c.-181_-180delinsTG	XP_011520798.1:n.-181_-180delinsTG
XM_024450280.1:c.-181_-180delinsTG	XP_024306048.1:n.-181_-180delinsTG
XM_024450281.1:c.-181_-180delinsTG	XP_024306049.1:n.-181_-180delinsTG
XR_001751904.1:n.365+10578_365+10579delinsTG
XR_002957860.1:n.1246+11164_1246+11165delinsCA
XR_002957861.1:n.1246+11164_1246+11165delinsCA
XR_002957863.1:n.1442+5868_1442+5869delinsCA
XR_932841.3:n.363+10578_363+10579delinsTG
XR_932842.2:n.363+10578_363+10579delinsTG
XR_932846.3:n.365+10578_365+10579delinsTG
XR_932847.3:n.365+10578_365+10579delinsTG