Canonical Allele Identifier: CA2207312842
Gene: CIITA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.10876966C= , CM000678.2:g.10876966C= GRCh38
NC_000016.9:g.10970823C= , CM000678.1:g.10970823C= GRCh37
NC_000016.8:g.10878324C= NCBI36
NG_009628.1:g.4769C= , LRG_49:g.4769C=

Transcript Alleles

HGVS Amino-acid change
ENST00000636238.1:c.-21+10647C= ENSP00000490205.1:n.-21+10647C=
ENST00000637439.1:c.283+10394C= ENSP00000489907.1:n.283+10394C=
XM_006720880.2:c.346+10394C= XP_006720943.2:n.346+10394C=
XM_011522484.1:c.346+10394C= XP_011520786.1:n.346+10394C=
XM_011522485.1:c.346+10394C= XP_011520787.1:n.346+10394C=
XM_011522486.1:c.346+10394C= XP_011520788.1:n.346+10394C=
XM_011522487.1:c.247+10394C= XP_011520789.1:n.247+10394C=
XM_011522489.1:c.247+10394C= XP_011520791.1:n.247+10394C=
XM_011522491.1:c.346+10394C= XP_011520793.1:n.346+10394C=
XM_011522494.1:c.-21+10647C= XP_011520796.1:n.-21+10647C=
XR_932841.1:n.361+10394C=
XR_932842.1:n.361+10394C=
XR_932843.1:n.361+10394C=
XR_932846.1:n.361+10394C=
XR_932847.1:n.361+10394C=
XR_933067.1:n.1162+11349G=
XR_933068.1:n.1162+11349G=
XM_006720880.3:c.346+10394C= XP_006720943.2:n.346+10394C=
XM_011522484.3:c.346+10394C= XP_011520786.1:n.346+10394C=
XM_011522485.2:c.346+10394C= XP_011520787.1:n.346+10394C=
XM_011522486.2:c.346+10394C= XP_011520788.1:n.346+10394C=
XM_011522487.2:c.247+10394C= XP_011520789.1:n.247+10394C=
XM_011522489.2:c.247+10394C= XP_011520791.1:n.247+10394C=
XM_011522491.2:c.346+10394C= XP_011520793.1:n.346+10394C=
XM_011522494.2:c.-21+10647C= XP_011520796.1:n.-21+10647C=
XR_001751904.1:n.365+10394C=
XR_002957860.1:n.1246+11349G=
XR_002957861.1:n.1246+11349G=
XR_002957863.1:n.1442+6053G=
XR_932841.3:n.363+10394C=
XR_932842.2:n.363+10394C=
XR_932846.3:n.365+10394C=
XR_932847.3:n.365+10394C=