Canonical Allele Identifier: CA2207313439
Gene: CIITA HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.10877997_10877998delinsGC , CM000678.2:g.10877997_10877998delinsGC GRCh38
NC_000016.9:g.10971854_10971855delinsGC , CM000678.1:g.10971854_10971855delinsGC GRCh37
NC_000016.8:g.10879355_10879356delinsGC NCBI36
NG_009628.1:g.5800_5801delinsGC , LRG_49:g.5800_5801delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000695878.1:n.157+615_157+616delinsGC
ENST00000324288.14:c.52+615_52+616delinsGC MANE Select ENSP00000316328.8:n.52+615_52+616delinsGC
ENST00000636238.1:c.-21+11678_-21+11679delinsGC ENSP00000490205.1:n.-21+11678_-21+11679delinsGC
ENST00000637439.1:c.283+11425_283+11426delinsGC ENSP00000489907.1:n.283+11425_283+11426delinsGC
ENST00000324288.12:c.52+615_52+616delinsGC ENSP00000316328.8:n.52+615_52+616delinsGC
ENST00000381835.9:c.52+615_52+616delinsGC ENSP00000371257.5:n.52+615_52+616delinsGC
ENST00000537380.1:n.52+615_52+616delinsGC
ENST00000570546.5:n.173+615_173+616delinsGC
ENST00000571186.5:c.52+615_52+616delinsGC ENSP00000459829.1:n.52+615_52+616delinsGC
ENST00000573309.5:n.167+615_167+616delinsGC
ENST00000611587.4:c.52+615_52+616delinsGC ENSP00000483487.1:n.52+615_52+616delinsGC
ENST00000618207.4:c.52+615_52+616delinsGC ENSP00000484761.1:n.52+615_52+616delinsGC
ENST00000618327.4:c.52+615_52+616delinsGC ENSP00000485010.1:n.52+615_52+616delinsGC
NM_000246.3:c.52+615_52+616delinsGC , LRG_49t1:c.52+615_52+616delinsGC NP_000237.2:n.52+615_52+616delinsGC
NM_001286402.1:c.52+615_52+616delinsGC NP_001273331.1:n.52+615_52+616delinsGC
NM_001286403.1:c.52+615_52+616delinsGC NP_001273332.1:n.52+615_52+616delinsGC
NR_104444.1:n.185+615_185+616delinsGC
XM_006720880.2:c.346+11425_346+11426delinsGC XP_006720943.2:n.346+11425_346+11426delinsGC
XM_011522484.1:c.346+11425_346+11426delinsGC XP_011520786.1:n.346+11425_346+11426delinsGC
XM_011522485.1:c.346+11425_346+11426delinsGC XP_011520787.1:n.346+11425_346+11426delinsGC
XM_011522486.1:c.346+11425_346+11426delinsGC XP_011520788.1:n.346+11425_346+11426delinsGC
XM_011522487.1:c.247+11425_247+11426delinsGC XP_011520789.1:n.247+11425_247+11426delinsGC
XM_011522489.1:c.247+11425_247+11426delinsGC XP_011520791.1:n.247+11425_247+11426delinsGC
XM_011522491.1:c.346+11425_346+11426delinsGC XP_011520793.1:n.346+11425_346+11426delinsGC
XM_011522492.1:c.52+615_52+616delinsGC XP_011520794.1:n.52+615_52+616delinsGC
XM_011522493.1:c.52+615_52+616delinsGC XP_011520795.1:n.52+615_52+616delinsGC
XM_011522494.1:c.-21+11678_-21+11679delinsGC XP_011520796.1:n.-21+11678_-21+11679delinsGC
XM_011522495.1:c.52+615_52+616delinsGC XP_011520797.1:n.52+615_52+616delinsGC
XM_011522496.1:c.52+615_52+616delinsGC XP_011520798.1:n.52+615_52+616delinsGC
XR_932841.1:n.361+11425_361+11426delinsGC
XR_932842.1:n.361+11425_361+11426delinsGC
XR_932843.1:n.361+11425_361+11426delinsGC
XR_932846.1:n.361+11425_361+11426delinsGC
XR_932847.1:n.361+11425_361+11426delinsGC
XR_932848.1:n.202+615_202+616delinsGC
XR_933067.1:n.1162+10317_1162+10318delinsGC
XR_933068.1:n.1162+10317_1162+10318delinsGC
XM_006720880.3:c.346+11425_346+11426delinsGC XP_006720943.2:n.346+11425_346+11426delinsGC
XM_011522484.3:c.346+11425_346+11426delinsGC XP_011520786.1:n.346+11425_346+11426delinsGC
XM_011522485.2:c.346+11425_346+11426delinsGC XP_011520787.1:n.346+11425_346+11426delinsGC
XM_011522486.2:c.346+11425_346+11426delinsGC XP_011520788.1:n.346+11425_346+11426delinsGC
XM_011522487.2:c.247+11425_247+11426delinsGC XP_011520789.1:n.247+11425_247+11426delinsGC
XM_011522488.2:c.-949_-948delinsGC XP_011520790.1:n.-949_-948delinsGC
XM_011522489.2:c.247+11425_247+11426delinsGC XP_011520791.1:n.247+11425_247+11426delinsGC
XM_011522490.2:c.-949_-948delinsGC XP_011520792.1:n.-949_-948delinsGC
XM_011522491.2:c.346+11425_346+11426delinsGC XP_011520793.1:n.346+11425_346+11426delinsGC
XM_011522492.2:c.52+615_52+616delinsGC XP_011520794.1:n.52+615_52+616delinsGC
XM_011522493.2:c.52+615_52+616delinsGC XP_011520795.1:n.52+615_52+616delinsGC
XM_011522494.2:c.-21+11678_-21+11679delinsGC XP_011520796.1:n.-21+11678_-21+11679delinsGC
XM_011522495.2:c.52+615_52+616delinsGC XP_011520797.1:n.52+615_52+616delinsGC
XM_011522496.2:c.52+615_52+616delinsGC XP_011520798.1:n.52+615_52+616delinsGC
XM_024450280.1:c.52+615_52+616delinsGC XP_024306048.1:n.52+615_52+616delinsGC
XM_024450281.1:c.52+615_52+616delinsGC XP_024306049.1:n.52+615_52+616delinsGC
XR_001751904.1:n.365+11425_365+11426delinsGC
XR_002957860.1:n.1246+10317_1246+10318delinsGC
XR_002957861.1:n.1246+10317_1246+10318delinsGC
XR_002957863.1:n.1442+5021_1442+5022delinsGC
XR_932841.3:n.363+11425_363+11426delinsGC
XR_932842.2:n.363+11425_363+11426delinsGC
XR_932846.3:n.365+11425_365+11426delinsGC
XR_932847.3:n.365+11425_365+11426delinsGC
NM_001286403.2:c.52+615_52+616delinsGC NP_001273332.1:n.52+615_52+616delinsGC
NR_104444.2:n.181+615_181+616delinsGC
NM_000246.4:c.52+615_52+616delinsGC MANE Select NP_000237.2:n.52+615_52+616delinsGC
NM_001379330.1:c.52+615_52+616delinsGC NP_001366259.1:n.52+615_52+616delinsGC
NM_001379331.1:c.52+615_52+616delinsGC NP_001366260.1:n.52+615_52+616delinsGC
NM_001379332.1:c.52+615_52+616delinsGC NP_001366261.1:n.52+615_52+616delinsGC
NM_001379333.1:c.52+615_52+616delinsGC NP_001366262.1:n.52+615_52+616delinsGC
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