Canonical Allele Identifier: CA16620064
Gene: CIITA HGNC NCBI

Linked Data

ClinVar Variation Id: 420718
dbSNP Id: rs1064794659

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.10907782del , CM000678.2:g.10907782del GRCh38
NC_000016.9:g.11001639del , CM000678.1:g.11001639del GRCh37
NC_000016.8:g.10909140del NCBI36
NG_009628.1:g.35585del , LRG_49:g.35585del

Transcript Alleles

HGVS Amino-acid change
ENST00000695879.1:n.2184del
ENST00000324288.14:c.2290del MANE Select ENSP00000316328.8:p.Gln764SerfsTer30
ENST00000324288.12:c.2290del ENSP00000316328.8:p.Gln764SerfsTer30
ENST00000381835.9:c.860-1201del ENSP00000371257.5:n.860-1201del
ENST00000537380.1:n.1007-2406del
ENST00000570546.5:n.2411del
ENST00000573309.5:n.2261del
ENST00000611587.4:c.2146del ENSP00000483487.1:p.Gln716SerfsTer30
ENST00000618207.4:c.1007-2406del ENSP00000484761.1:n.1007-2406del
ENST00000618327.4:c.2293del ENSP00000485010.1:p.Gln765SerfsTer30
NM_000246.3:c.2290del , LRG_49t1:c.2290del NP_000237.2:p.Gln764SerfsTer30
NM_001286402.1:c.2293del NP_001273331.1:p.Gln765SerfsTer30
NM_001286403.1:c.860-1201del NP_001273332.1:n.860-1201del
NR_104444.1:n.1140-2406del
XM_006720880.2:c.2587del XP_006720943.2:p.Gln863SerfsTer30
XM_011522484.1:c.2587del XP_011520786.1:p.Gln863SerfsTer30
XM_011522485.1:c.2587del XP_011520787.1:p.Gln863SerfsTer30
XM_011522486.1:c.2587del XP_011520788.1:p.Gln863SerfsTer30
XM_011522487.1:c.2341del XP_011520789.1:p.Gln781SerfsTer30
XM_011522488.1:c.2338del XP_011520790.1:p.Gln780SerfsTer30
XM_011522489.1:c.2338del XP_011520791.1:p.Gln780SerfsTer30
XM_011522490.1:c.2335del XP_011520792.1:p.Gln779SerfsTer30
XM_011522491.1:c.2587del XP_011520793.1:p.Gln863SerfsTer30
XM_011522492.1:c.2293del XP_011520794.1:p.Gln765SerfsTer30
XM_011522493.1:c.2290del XP_011520795.1:p.Gln764SerfsTer30
XM_011522494.1:c.2221del XP_011520796.1:p.Gln741SerfsTer30
XM_011522495.1:c.2146del XP_011520797.1:p.Gln716SerfsTer30
XM_011522496.1:c.2143del XP_011520798.1:p.Gln715SerfsTer30
XR_932841.1:n.2602del
XR_932842.1:n.2602del
XR_932843.1:n.2602del
XR_932846.1:n.2602del
XR_932847.1:n.2602del
XR_932848.1:n.1010-1201del
XM_006720880.3:c.2587del XP_006720943.2:p.Gln863SerfsTer30
XM_011522484.3:c.2587del XP_011520786.1:p.Gln863SerfsTer30
XM_011522485.2:c.2587del XP_011520787.1:p.Gln863SerfsTer30
XM_011522486.2:c.2587del XP_011520788.1:p.Gln863SerfsTer30
XM_011522487.2:c.2341del XP_011520789.1:p.Gln781SerfsTer30
XM_011522488.2:c.2338del XP_011520790.1:p.Gln780SerfsTer30
XM_011522489.2:c.2338del XP_011520791.1:p.Gln780SerfsTer30
XM_011522490.2:c.2335del XP_011520792.1:p.Gln779SerfsTer30
XM_011522491.2:c.2587del XP_011520793.1:p.Gln863SerfsTer30
XM_011522492.2:c.2293del XP_011520794.1:p.Gln765SerfsTer30
XM_011522493.2:c.2290del XP_011520795.1:p.Gln764SerfsTer30
XM_011522494.2:c.2221del XP_011520796.1:p.Gln741SerfsTer30
XM_011522495.2:c.2146del XP_011520797.1:p.Gln716SerfsTer30
XM_011522496.2:c.2143del XP_011520798.1:p.Gln715SerfsTer30
XM_024450280.1:c.2533del XP_024306048.1:p.Gln845SerfsTer30
XM_024450281.1:c.2386del XP_024306049.1:p.Gln796SerfsTer30
XR_001751904.1:n.2606del
XR_932841.3:n.2604del
XR_932842.2:n.2604del
XR_932846.3:n.2606del
XR_932847.3:n.2606del
NM_001286403.2:c.860-1201del NP_001273332.1:n.860-1201del
NR_104444.2:n.1136-2406del
NM_000246.4:c.2290del MANE Select NP_000237.2:p.Gln764SerfsTer30
NM_001379330.1:c.2146del NP_001366259.1:p.Gln716SerfsTer30
NM_001379331.1:c.2143del NP_001366260.1:p.Gln715SerfsTer30
NM_001379332.1:c.2293del NP_001366261.1:p.Gln765SerfsTer30
NM_001379333.1:c.2290del NP_001366262.1:p.Gln764SerfsTer30
NM_001379334.1:c.2221del NP_001366263.1:p.Gln741SerfsTer30