Canonical Allele Identifier: CA2207312840
Gene: CIITA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.10876965C= , CM000678.2:g.10876965C= GRCh38
NC_000016.9:g.10970822C= , CM000678.1:g.10970822C= GRCh37
NC_000016.8:g.10878323C= NCBI36
NG_009628.1:g.4768C= , LRG_49:g.4768C=

Transcript Alleles

HGVS Amino-acid change
ENST00000636238.1:c.-21+10646C= ENSP00000490205.1:n.-21+10646C=
ENST00000637439.1:c.283+10393C= ENSP00000489907.1:n.283+10393C=
XM_006720880.2:c.346+10393C= XP_006720943.2:n.346+10393C=
XM_011522484.1:c.346+10393C= XP_011520786.1:n.346+10393C=
XM_011522485.1:c.346+10393C= XP_011520787.1:n.346+10393C=
XM_011522486.1:c.346+10393C= XP_011520788.1:n.346+10393C=
XM_011522487.1:c.247+10393C= XP_011520789.1:n.247+10393C=
XM_011522489.1:c.247+10393C= XP_011520791.1:n.247+10393C=
XM_011522491.1:c.346+10393C= XP_011520793.1:n.346+10393C=
XM_011522494.1:c.-21+10646C= XP_011520796.1:n.-21+10646C=
XR_932841.1:n.361+10393C=
XR_932842.1:n.361+10393C=
XR_932843.1:n.361+10393C=
XR_932846.1:n.361+10393C=
XR_932847.1:n.361+10393C=
XR_933067.1:n.1162+11350G=
XR_933068.1:n.1162+11350G=
XM_006720880.3:c.346+10393C= XP_006720943.2:n.346+10393C=
XM_011522484.3:c.346+10393C= XP_011520786.1:n.346+10393C=
XM_011522485.2:c.346+10393C= XP_011520787.1:n.346+10393C=
XM_011522486.2:c.346+10393C= XP_011520788.1:n.346+10393C=
XM_011522487.2:c.247+10393C= XP_011520789.1:n.247+10393C=
XM_011522489.2:c.247+10393C= XP_011520791.1:n.247+10393C=
XM_011522491.2:c.346+10393C= XP_011520793.1:n.346+10393C=
XM_011522494.2:c.-21+10646C= XP_011520796.1:n.-21+10646C=
XR_001751904.1:n.365+10393C=
XR_002957860.1:n.1246+11350G=
XR_002957861.1:n.1246+11350G=
XR_002957863.1:n.1442+6054G=
XR_932841.3:n.363+10393C=
XR_932842.2:n.363+10393C=
XR_932846.3:n.365+10393C=
XR_932847.3:n.365+10393C=