Canonical Allele Identifier: CA2207323774

Gene: CIITA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10906539_10906540delinsTG , CM000678.2:g.10906539_10906540delinsTG	GRCh38
NC_000016.9:g.11000396_11000397delinsTG , CM000678.1:g.11000396_11000397delinsTG	GRCh37
NC_000016.8:g.10907897_10907898delinsTG	NCBI36
NG_009628.1:g.34342_34343delinsTG , LRG_49:g.34342_34343delinsTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000695879.1:n.1072_1073delinsTG
ENST00000324288.14:c.1047_1048delinsTG MANE Select	ENSP00000316328.8:p.Tyr349=
ENST00000324288.12:c.1047_1048delinsTG	ENSP00000316328.8:p.Tyr349=
ENST00000381835.9:c.859+1727_859+1728delinsTG	ENSP00000371257.5:n.859+1727_859+1728delinsTG
ENST00000537380.1:n.1006+1727_1006+1728delinsTG
ENST00000570546.5:n.1168_1169delinsTG
ENST00000573309.5:n.1018_1019delinsTG
ENST00000611587.4:c.903_904delinsTG	ENSP00000483487.1:p.Tyr301=
ENST00000618207.4:c.1006+1727_1006+1728delinsTG	ENSP00000484761.1:n.1006+1727_1006+1728delinsTG
ENST00000618327.4:c.1050_1051delinsTG	ENSP00000485010.1:p.Tyr350=
NM_000246.3:c.1047_1048delinsTG , LRG_49t1:c.1047_1048delinsTG	NP_000237.2:p.Tyr349=
NM_001286402.1:c.1050_1051delinsTG	NP_001273331.1:p.Tyr350=
NM_001286403.1:c.859+1727_859+1728delinsTG	NP_001273332.1:n.859+1727_859+1728delinsTG
NR_104444.1:n.1139+1727_1139+1728delinsTG
XM_006720880.2:c.1344_1345delinsTG	XP_006720943.2:p.Tyr448=
XM_011522484.1:c.1344_1345delinsTG	XP_011520786.1:p.Tyr448=
XM_011522485.1:c.1344_1345delinsTG	XP_011520787.1:p.Tyr448=
XM_011522486.1:c.1344_1345delinsTG	XP_011520788.1:p.Tyr448=
XM_011522487.1:c.1098_1099delinsTG	XP_011520789.1:p.Tyr366=
XM_011522488.1:c.1095_1096delinsTG	XP_011520790.1:p.Tyr365=
XM_011522489.1:c.1095_1096delinsTG	XP_011520791.1:p.Tyr365=
XM_011522490.1:c.1092_1093delinsTG	XP_011520792.1:p.Tyr364=
XM_011522491.1:c.1344_1345delinsTG	XP_011520793.1:p.Tyr448=
XM_011522492.1:c.1050_1051delinsTG	XP_011520794.1:p.Tyr350=
XM_011522493.1:c.1047_1048delinsTG	XP_011520795.1:p.Tyr349=
XM_011522494.1:c.978_979delinsTG	XP_011520796.1:p.Tyr326=
XM_011522495.1:c.903_904delinsTG	XP_011520797.1:p.Tyr301=
XM_011522496.1:c.900_901delinsTG	XP_011520798.1:p.Tyr300=
XR_932841.1:n.1359_1360delinsTG
XR_932842.1:n.1359_1360delinsTG
XR_932843.1:n.1359_1360delinsTG
XR_932846.1:n.1359_1360delinsTG
XR_932847.1:n.1359_1360delinsTG
XR_932848.1:n.1009+1727_1009+1728delinsTG
XM_006720880.3:c.1344_1345delinsTG	XP_006720943.2:p.Tyr448=
XM_011522484.3:c.1344_1345delinsTG	XP_011520786.1:p.Tyr448=
XM_011522485.2:c.1344_1345delinsTG	XP_011520787.1:p.Tyr448=
XM_011522486.2:c.1344_1345delinsTG	XP_011520788.1:p.Tyr448=
XM_011522487.2:c.1098_1099delinsTG	XP_011520789.1:p.Tyr366=
XM_011522488.2:c.1095_1096delinsTG	XP_011520790.1:p.Tyr365=
XM_011522489.2:c.1095_1096delinsTG	XP_011520791.1:p.Tyr365=
XM_011522490.2:c.1092_1093delinsTG	XP_011520792.1:p.Tyr364=
XM_011522491.2:c.1344_1345delinsTG	XP_011520793.1:p.Tyr448=
XM_011522492.2:c.1050_1051delinsTG	XP_011520794.1:p.Tyr350=
XM_011522493.2:c.1047_1048delinsTG	XP_011520795.1:p.Tyr349=
XM_011522494.2:c.978_979delinsTG	XP_011520796.1:p.Tyr326=
XM_011522495.2:c.903_904delinsTG	XP_011520797.1:p.Tyr301=
XM_011522496.2:c.900_901delinsTG	XP_011520798.1:p.Tyr300=
XM_024450280.1:c.1290_1291delinsTG	XP_024306048.1:p.Tyr430=
XM_024450281.1:c.1143_1144delinsTG	XP_024306049.1:p.Tyr381=
XR_001751904.1:n.1363_1364delinsTG
XR_932841.3:n.1361_1362delinsTG
XR_932842.2:n.1361_1362delinsTG
XR_932846.3:n.1363_1364delinsTG
XR_932847.3:n.1363_1364delinsTG
NM_001286403.2:c.859+1727_859+1728delinsTG	NP_001273332.1:n.859+1727_859+1728delinsTG
NR_104444.2:n.1135+1727_1135+1728delinsTG
NM_000246.4:c.1047_1048delinsTG MANE Select	NP_000237.2:p.Tyr349=
NM_001379330.1:c.903_904delinsTG	NP_001366259.1:p.Tyr301=
NM_001379331.1:c.900_901delinsTG	NP_001366260.1:p.Tyr300=
NM_001379332.1:c.1050_1051delinsTG	NP_001366261.1:p.Tyr350=
NM_001379333.1:c.1047_1048delinsTG	NP_001366262.1:p.Tyr349=
NM_001379334.1:c.978_979delinsTG	NP_001366263.1:p.Tyr326=