Canonical Allele Identifier: CA2207318965

Gene: CIITA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10902137_10902148delinsAGCCAGCCTCCG , CM000678.2:g.10902137_10902148delinsAGCCAGCCTCCG	GRCh38
NC_000016.9:g.10995994_10996005delinsAGCCAGCCTCCG , CM000678.1:g.10995994_10996005delinsAGCCAGCCTCCG	GRCh37
NC_000016.8:g.10903495_10903506delinsAGCCAGCCTCCG	NCBI36
NG_009628.1:g.29940_29951delinsAGCCAGCCTCCG , LRG_49:g.29940_29951delinsAGCCAGCCTCCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695879.1:n.606_617delinsAGCCAGCCTCCG
ENST00000324288.14:c.581_592delinsAGCCAGCCTCCG MANE Select	ENSP00000316328.8:p.Glu194=
ENST00000324288.12:c.581_592delinsAGCCAGCCTCCG	ENSP00000316328.8:p.Glu194=
ENST00000381835.9:c.482-521_482-510delinsAGCCAGCCTCCG	ENSP00000371257.5:n.482-521_482-510delinsAGCCAGCCTCCG
ENST00000537380.1:n.581_592delinsAGCCAGCCTCCG
ENST00000570546.5:n.702_713delinsAGCCAGCCTCCG
ENST00000571186.5:c.*302_*313delinsAGCCAGCCTCCG	ENSP00000459829.1:n.*302_*313delinsAGCCAGCCTCCG
ENST00000573309.5:n.600-521_600-510delinsAGCCAGCCTCCG
ENST00000576601.1:c.509_520delinsAGCCAGCCTCCG	ENSP00000459608.1:p.Glu170=
ENST00000611587.4:c.485-521_485-510delinsAGCCAGCCTCCG	ENSP00000483487.1:n.485-521_485-510delinsAGCCAGCCTCCG
ENST00000618207.4:c.581_592delinsAGCCAGCCTCCG	ENSP00000484761.1:p.Glu194=
ENST00000618327.4:c.584_595delinsAGCCAGCCTCCG	ENSP00000485010.1:p.Glu195=
NM_000246.3:c.581_592delinsAGCCAGCCTCCG , LRG_49t1:c.581_592delinsAGCCAGCCTCCG	NP_000237.2:p.Glu194=
NM_001286402.1:c.584_595delinsAGCCAGCCTCCG	NP_001273331.1:p.Glu195=
NM_001286403.1:c.482-521_482-510delinsAGCCAGCCTCCG	NP_001273332.1:n.482-521_482-510delinsAGCCAGCCTCCG
NR_104444.1:n.714_725delinsAGCCAGCCTCCG
XM_006720880.2:c.878_889delinsAGCCAGCCTCCG	XP_006720943.2:p.Glu293=
XM_011522484.1:c.878_889delinsAGCCAGCCTCCG	XP_011520786.1:p.Glu293=
XM_011522485.1:c.878_889delinsAGCCAGCCTCCG	XP_011520787.1:p.Glu293=
XM_011522486.1:c.878_889delinsAGCCAGCCTCCG	XP_011520788.1:p.Glu293=
XM_011522487.1:c.680-521_680-510delinsAGCCAGCCTCCG	XP_011520789.1:n.680-521_680-510delinsAGCCAGCCTCCG
XM_011522488.1:c.629_640delinsAGCCAGCCTCCG	XP_011520790.1:p.Glu210=
XM_011522489.1:c.677-521_677-510delinsAGCCAGCCTCCG	XP_011520791.1:n.677-521_677-510delinsAGCCAGCCTCCG
XM_011522490.1:c.626_637delinsAGCCAGCCTCCG	XP_011520792.1:p.Glu209=
XM_011522491.1:c.878_889delinsAGCCAGCCTCCG	XP_011520793.1:p.Glu293=
XM_011522492.1:c.584_595delinsAGCCAGCCTCCG	XP_011520794.1:p.Glu195=
XM_011522493.1:c.581_592delinsAGCCAGCCTCCG	XP_011520795.1:p.Glu194=
XM_011522494.1:c.512_523delinsAGCCAGCCTCCG	XP_011520796.1:p.Glu171=
XM_011522495.1:c.485-521_485-510delinsAGCCAGCCTCCG	XP_011520797.1:n.485-521_485-510delinsAGCCAGCCTCCG
XM_011522496.1:c.482-521_482-510delinsAGCCAGCCTCCG	XP_011520798.1:n.482-521_482-510delinsAGCCAGCCTCCG
XR_932841.1:n.893_904delinsAGCCAGCCTCCG
XR_932842.1:n.893_904delinsAGCCAGCCTCCG
XR_932843.1:n.893_904delinsAGCCAGCCTCCG
XR_932846.1:n.893_904delinsAGCCAGCCTCCG
XR_932847.1:n.893_904delinsAGCCAGCCTCCG
XR_932848.1:n.632-521_632-510delinsAGCCAGCCTCCG
XM_006720880.3:c.878_889delinsAGCCAGCCTCCG	XP_006720943.2:p.Glu293=
XM_011522484.3:c.878_889delinsAGCCAGCCTCCG	XP_011520786.1:p.Glu293=
XM_011522485.2:c.878_889delinsAGCCAGCCTCCG	XP_011520787.1:p.Glu293=
XM_011522486.2:c.878_889delinsAGCCAGCCTCCG	XP_011520788.1:p.Glu293=
XM_011522487.2:c.680-521_680-510delinsAGCCAGCCTCCG	XP_011520789.1:n.680-521_680-510delinsAGCCAGCCTCCG
XM_011522488.2:c.629_640delinsAGCCAGCCTCCG	XP_011520790.1:p.Glu210=
XM_011522489.2:c.677-521_677-510delinsAGCCAGCCTCCG	XP_011520791.1:n.677-521_677-510delinsAGCCAGCCTCCG
XM_011522490.2:c.626_637delinsAGCCAGCCTCCG	XP_011520792.1:p.Glu209=
XM_011522491.2:c.878_889delinsAGCCAGCCTCCG	XP_011520793.1:p.Glu293=
XM_011522492.2:c.584_595delinsAGCCAGCCTCCG	XP_011520794.1:p.Glu195=
XM_011522493.2:c.581_592delinsAGCCAGCCTCCG	XP_011520795.1:p.Glu194=
XM_011522494.2:c.512_523delinsAGCCAGCCTCCG	XP_011520796.1:p.Glu171=
XM_011522495.2:c.485-521_485-510delinsAGCCAGCCTCCG	XP_011520797.1:n.485-521_485-510delinsAGCCAGCCTCCG
XM_011522496.2:c.482-521_482-510delinsAGCCAGCCTCCG	XP_011520798.1:n.482-521_482-510delinsAGCCAGCCTCCG
XM_024450280.1:c.824_835delinsAGCCAGCCTCCG	XP_024306048.1:p.Glu275=
XM_024450281.1:c.725-521_725-510delinsAGCCAGCCTCCG	XP_024306049.1:n.725-521_725-510delinsAGCCAGCCTCCG
XR_001751904.1:n.897_908delinsAGCCAGCCTCCG
XR_932841.3:n.895_906delinsAGCCAGCCTCCG
XR_932842.2:n.895_906delinsAGCCAGCCTCCG
XR_932846.3:n.897_908delinsAGCCAGCCTCCG
XR_932847.3:n.897_908delinsAGCCAGCCTCCG
NM_001286403.2:c.482-521_482-510delinsAGCCAGCCTCCG	NP_001273332.1:n.482-521_482-510delinsAGCCAGCCTCCG
NR_104444.2:n.710_721delinsAGCCAGCCTCCG
NM_000246.4:c.581_592delinsAGCCAGCCTCCG MANE Select	NP_000237.2:p.Glu194=
NM_001379330.1:c.485-521_485-510delinsAGCCAGCCTCCG	NP_001366259.1:n.485-521_485-510delinsAGCCAGCCTCCG
NM_001379331.1:c.482-521_482-510delinsAGCCAGCCTCCG	NP_001366260.1:n.482-521_482-510delinsAGCCAGCCTCCG
NM_001379332.1:c.584_595delinsAGCCAGCCTCCG	NP_001366261.1:p.Glu195=
NM_001379333.1:c.581_592delinsAGCCAGCCTCCG	NP_001366262.1:p.Glu194=
NM_001379334.1:c.512_523delinsAGCCAGCCTCCG	NP_001366263.1:p.Glu171=