Canonical Allele Identifier: CA717939587

Gene: CIITA

Linked Data

• dbSNP Id: rs1468022512
• MyVariant Identifiers: chr16:g.11002962_11002964del (hg19) ; chr16:g.10909105_10909107del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10909108_10909110del , CM000678.2:g.10909108_10909110del	GRCh38
NC_000016.9:g.11002965_11002967del , CM000678.1:g.11002965_11002967del	GRCh37
NC_000016.8:g.10910466_10910468del	NCBI36
NG_009628.1:g.36911_36913del , LRG_49:g.36911_36913del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324288.14:c.2737_2739del MANE Select	ENSP00000316328.8:p.Glu913del
ENST00000324288.12:c.2737_2739del	ENSP00000316328.8:p.Glu913del
ENST00000381835.9:c.985_987del	ENSP00000371257.5:p.Glu329del
ENST00000537380.1:n.1007-1080_1007-1078del
ENST00000570546.5:n.3737_3739del
ENST00000618207.4:c.1007-1080_1007-1078del	ENSP00000484761.1:n.1007-1080_1007-1078del
ENST00000618327.4:c.2740_2742del	ENSP00000485010.1:p.Glu914del
NM_000246.3:c.2737_2739del , LRG_49t1:c.2737_2739del	NP_000237.2:p.Glu913del
NM_001286402.1:c.2740_2742del	NP_001273331.1:p.Glu914del
NM_001286403.1:c.985_987del	NP_001273332.1:p.Glu329del
NR_104444.1:n.1140-1080_1140-1078del
XM_006720880.2:c.3034_3036del	XP_006720943.2:p.Glu1012del
XM_011522484.1:c.3034_3036del	XP_011520786.1:p.Glu1012del
XM_011522485.1:c.3034_3036del	XP_011520787.1:p.Glu1012del
XM_011522486.1:c.3034_3036del	XP_011520788.1:p.Glu1012del
XM_011522487.1:c.2788_2790del	XP_011520789.1:p.Glu930del
XM_011522488.1:c.2785_2787del	XP_011520790.1:p.Glu929del
XM_011522489.1:c.2785_2787del	XP_011520791.1:p.Glu929del
XM_011522490.1:c.2782_2784del	XP_011520792.1:p.Glu928del
XM_011522491.1:c.3034_3036del	XP_011520793.1:p.Glu1012del
XM_011522492.1:c.2740_2742del	XP_011520794.1:p.Glu914del
XM_011522493.1:c.2737_2739del	XP_011520795.1:p.Glu913del
XM_011522494.1:c.2668_2670del	XP_011520796.1:p.Glu890del
XM_011522495.1:c.2593_2595del	XP_011520797.1:p.Glu865del
XM_011522496.1:c.2590_2592del	XP_011520798.1:p.Glu864del
XR_932841.1:n.3049_3051del
XR_932842.1:n.3049_3051del
XR_932843.1:n.3049_3051del
XR_932846.1:n.3095_3097del
XR_932847.1:n.3095_3097del
XR_932848.1:n.1135_1137del
XM_006720880.3:c.3034_3036del	XP_006720943.2:p.Glu1012del
XM_011522484.3:c.3034_3036del	XP_011520786.1:p.Glu1012del
XM_011522485.2:c.3034_3036del	XP_011520787.1:p.Glu1012del
XM_011522486.2:c.3034_3036del	XP_011520788.1:p.Glu1012del
XM_011522487.2:c.2788_2790del	XP_011520789.1:p.Glu930del
XM_011522488.2:c.2785_2787del	XP_011520790.1:p.Glu929del
XM_011522489.2:c.2785_2787del	XP_011520791.1:p.Glu929del
XM_011522490.2:c.2782_2784del	XP_011520792.1:p.Glu928del
XM_011522491.2:c.3034_3036del	XP_011520793.1:p.Glu1012del
XM_011522492.2:c.2740_2742del	XP_011520794.1:p.Glu914del
XM_011522493.2:c.2737_2739del	XP_011520795.1:p.Glu913del
XM_011522494.2:c.2668_2670del	XP_011520796.1:p.Glu890del
XM_011522495.2:c.2593_2595del	XP_011520797.1:p.Glu865del
XM_011522496.2:c.2590_2592del	XP_011520798.1:p.Glu864del
XM_024450280.1:c.2980_2982del	XP_024306048.1:p.Glu994del
XM_024450281.1:c.2833_2835del	XP_024306049.1:p.Glu945del
XR_001751904.1:n.3099_3101del
XR_932841.3:n.3051_3053del
XR_932842.2:n.3051_3053del
XR_932846.3:n.3099_3101del
XR_932847.3:n.3099_3101del
NM_001286403.2:c.985_987del	NP_001273332.1:p.Glu329del
NR_104444.2:n.1136-1080_1136-1078del
NM_000246.4:c.2737_2739del MANE Select	NP_000237.2:p.Glu913del
NM_001379330.1:c.2593_2595del	NP_001366259.1:p.Glu865del
NM_001379331.1:c.2590_2592del	NP_001366260.1:p.Glu864del
NM_001379332.1:c.2740_2742del	NP_001366261.1:p.Glu914del
NM_001379333.1:c.2737_2739del	NP_001366262.1:p.Glu913del
NM_001379334.1:c.2668_2670del	NP_001366263.1:p.Glu890del