Canonical Allele Identifier: CA16518737
Gene: CIITA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.10900325G>A , CM000678.2:g.10900325G>A GRCh38
NC_000016.9:g.10994182G>A , CM000678.1:g.10994182G>A GRCh37
NC_000016.8:g.10901683G>A NCBI36
NG_009628.1:g.28128G>A , LRG_49:g.28128G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000695878.1:n.2107G>A
ENST00000695879.1:n.462-1189G>A
ENST00000324288.14:c.437-1189G>A MANE Select ENSP00000316328.8:n.437-1189G>A
ENST00000636238.1:c.368-1189G>A ENSP00000490205.1:n.368-1189G>A
ENST00000637439.1:c.671-1189G>A ENSP00000489907.1:n.671-1189G>A
ENST00000324288.12:c.437-1189G>A ENSP00000316328.8:n.437-1189G>A
ENST00000381835.9:c.437-1189G>A ENSP00000371257.5:n.437-1189G>A
ENST00000537380.1:n.437-1189G>A
ENST00000570546.5:n.558-1189G>A
ENST00000571186.5:c.437-1189G>A ENSP00000459829.1:n.437-1189G>A
ENST00000573309.5:n.555-1189G>A
ENST00000576601.1:c.365-1189G>A ENSP00000459608.1:n.365-1189G>A
ENST00000611587.4:c.440-1189G>A ENSP00000483487.1:n.440-1189G>A
ENST00000618207.4:c.437-1189G>A ENSP00000484761.1:n.437-1189G>A
ENST00000618327.4:c.440-1189G>A ENSP00000485010.1:n.440-1189G>A
NM_000246.3:c.437-1189G>A , LRG_49t1:c.437-1189G>A NP_000237.2:n.437-1189G>A
NM_001286402.1:c.440-1189G>A NP_001273331.1:n.440-1189G>A
NM_001286403.1:c.437-1189G>A NP_001273332.1:n.437-1189G>A
NR_104444.1:n.570-1189G>A
XM_006720880.2:c.734-1189G>A XP_006720943.2:n.734-1189G>A
XM_011522484.1:c.734-1189G>A XP_011520786.1:n.734-1189G>A
XM_011522485.1:c.734-1189G>A XP_011520787.1:n.734-1189G>A
XM_011522486.1:c.734-1189G>A XP_011520788.1:n.734-1189G>A
XM_011522487.1:c.635-1189G>A XP_011520789.1:n.635-1189G>A
XM_011522488.1:c.485-1189G>A XP_011520790.1:n.485-1189G>A
XM_011522489.1:c.632-1189G>A XP_011520791.1:n.632-1189G>A
XM_011522490.1:c.482-1189G>A XP_011520792.1:n.482-1189G>A
XM_011522491.1:c.734-1189G>A XP_011520793.1:n.734-1189G>A
XM_011522492.1:c.440-1189G>A XP_011520794.1:n.440-1189G>A
XM_011522493.1:c.437-1189G>A XP_011520795.1:n.437-1189G>A
XM_011522494.1:c.368-1189G>A XP_011520796.1:n.368-1189G>A
XM_011522495.1:c.440-1189G>A XP_011520797.1:n.440-1189G>A
XM_011522496.1:c.437-1189G>A XP_011520798.1:n.437-1189G>A
XR_932841.1:n.749-1189G>A
XR_932842.1:n.749-1189G>A
XR_932843.1:n.749-1189G>A
XR_932846.1:n.749-1189G>A
XR_932847.1:n.749-1189G>A
XR_932848.1:n.587-1189G>A
XM_006720880.3:c.734-1189G>A XP_006720943.2:n.734-1189G>A
XM_011522484.3:c.734-1189G>A XP_011520786.1:n.734-1189G>A
XM_011522485.2:c.734-1189G>A XP_011520787.1:n.734-1189G>A
XM_011522486.2:c.734-1189G>A XP_011520788.1:n.734-1189G>A
XM_011522487.2:c.635-1189G>A XP_011520789.1:n.635-1189G>A
XM_011522488.2:c.485-1189G>A XP_011520790.1:n.485-1189G>A
XM_011522489.2:c.632-1189G>A XP_011520791.1:n.632-1189G>A
XM_011522490.2:c.482-1189G>A XP_011520792.1:n.482-1189G>A
XM_011522491.2:c.734-1189G>A XP_011520793.1:n.734-1189G>A
XM_011522492.2:c.440-1189G>A XP_011520794.1:n.440-1189G>A
XM_011522493.2:c.437-1189G>A XP_011520795.1:n.437-1189G>A
XM_011522494.2:c.368-1189G>A XP_011520796.1:n.368-1189G>A
XM_011522495.2:c.440-1189G>A XP_011520797.1:n.440-1189G>A
XM_011522496.2:c.437-1189G>A XP_011520798.1:n.437-1189G>A
XM_024450280.1:c.680-1189G>A XP_024306048.1:n.680-1189G>A
XM_024450281.1:c.680-1189G>A XP_024306049.1:n.680-1189G>A
XR_001751904.1:n.753-1189G>A
XR_932841.3:n.751-1189G>A
XR_932842.2:n.751-1189G>A
XR_932846.3:n.753-1189G>A
XR_932847.3:n.753-1189G>A
NM_001286403.2:c.437-1189G>A NP_001273332.1:n.437-1189G>A
NR_104444.2:n.566-1189G>A
NM_000246.4:c.437-1189G>A MANE Select NP_000237.2:n.437-1189G>A
NM_001379330.1:c.440-1189G>A NP_001366259.1:n.440-1189G>A
NM_001379331.1:c.437-1189G>A NP_001366260.1:n.437-1189G>A
NM_001379332.1:c.440-1189G>A NP_001366261.1:n.440-1189G>A
NM_001379333.1:c.437-1189G>A NP_001366262.1:n.437-1189G>A
NM_001379334.1:c.368-1189G>A NP_001366263.1:n.368-1189G>A
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