Canonical Allele Identifier: CA394729677

Gene: CIITA

Linked Data

• MyVariant Identifiers: chr16:g.11000401C>A (hg19) ; chr16:g.10906544C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10906544C>A , CM000678.2:g.10906544C>A	GRCh38
NC_000016.9:g.11000401C>A , CM000678.1:g.11000401C>A	GRCh37
NC_000016.8:g.10907902C>A	NCBI36
NG_009628.1:g.34347C>A , LRG_49:g.34347C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000695879.1:n.1077C>A
ENST00000324288.14:c.1052C>A MANE Select	ENSP00000316328.8:p.Ala351Asp
ENST00000324288.12:c.1052C>A	ENSP00000316328.8:p.Ala351Asp
ENST00000381835.9:c.859+1732C>A	ENSP00000371257.5:n.859+1732C>A
ENST00000537380.1:n.1006+1732C>A
ENST00000570546.5:n.1173C>A
ENST00000573309.5:n.1023C>A
ENST00000611587.4:c.908C>A	ENSP00000483487.1:p.Ala303Asp
ENST00000618207.4:c.1006+1732C>A	ENSP00000484761.1:n.1006+1732C>A
ENST00000618327.4:c.1055C>A	ENSP00000485010.1:p.Ala352Asp
NM_000246.3:c.1052C>A , LRG_49t1:c.1052C>A	NP_000237.2:p.Ala351Asp
NM_001286402.1:c.1055C>A	NP_001273331.1:p.Ala352Asp
NM_001286403.1:c.859+1732C>A	NP_001273332.1:n.859+1732C>A
NR_104444.1:n.1139+1732C>A
XM_006720880.2:c.1349C>A	XP_006720943.2:p.Ala450Asp
XM_011522484.1:c.1349C>A	XP_011520786.1:p.Ala450Asp
XM_011522485.1:c.1349C>A	XP_011520787.1:p.Ala450Asp
XM_011522486.1:c.1349C>A	XP_011520788.1:p.Ala450Asp
XM_011522487.1:c.1103C>A	XP_011520789.1:p.Ala368Asp
XM_011522488.1:c.1100C>A	XP_011520790.1:p.Ala367Asp
XM_011522489.1:c.1100C>A	XP_011520791.1:p.Ala367Asp
XM_011522490.1:c.1097C>A	XP_011520792.1:p.Ala366Asp
XM_011522491.1:c.1349C>A	XP_011520793.1:p.Ala450Asp
XM_011522492.1:c.1055C>A	XP_011520794.1:p.Ala352Asp
XM_011522493.1:c.1052C>A	XP_011520795.1:p.Ala351Asp
XM_011522494.1:c.983C>A	XP_011520796.1:p.Ala328Asp
XM_011522495.1:c.908C>A	XP_011520797.1:p.Ala303Asp
XM_011522496.1:c.905C>A	XP_011520798.1:p.Ala302Asp
XR_932841.1:n.1364C>A
XR_932842.1:n.1364C>A
XR_932843.1:n.1364C>A
XR_932846.1:n.1364C>A
XR_932847.1:n.1364C>A
XR_932848.1:n.1009+1732C>A
XM_006720880.3:c.1349C>A	XP_006720943.2:p.Ala450Asp
XM_011522484.3:c.1349C>A	XP_011520786.1:p.Ala450Asp
XM_011522485.2:c.1349C>A	XP_011520787.1:p.Ala450Asp
XM_011522486.2:c.1349C>A	XP_011520788.1:p.Ala450Asp
XM_011522487.2:c.1103C>A	XP_011520789.1:p.Ala368Asp
XM_011522488.2:c.1100C>A	XP_011520790.1:p.Ala367Asp
XM_011522489.2:c.1100C>A	XP_011520791.1:p.Ala367Asp
XM_011522490.2:c.1097C>A	XP_011520792.1:p.Ala366Asp
XM_011522491.2:c.1349C>A	XP_011520793.1:p.Ala450Asp
XM_011522492.2:c.1055C>A	XP_011520794.1:p.Ala352Asp
XM_011522493.2:c.1052C>A	XP_011520795.1:p.Ala351Asp
XM_011522494.2:c.983C>A	XP_011520796.1:p.Ala328Asp
XM_011522495.2:c.908C>A	XP_011520797.1:p.Ala303Asp
XM_011522496.2:c.905C>A	XP_011520798.1:p.Ala302Asp
XM_024450280.1:c.1295C>A	XP_024306048.1:p.Ala432Asp
XM_024450281.1:c.1148C>A	XP_024306049.1:p.Ala383Asp
XR_001751904.1:n.1368C>A
XR_932841.3:n.1366C>A
XR_932842.2:n.1366C>A
XR_932846.3:n.1368C>A
XR_932847.3:n.1368C>A
NM_001286403.2:c.859+1732C>A	NP_001273332.1:n.859+1732C>A
NR_104444.2:n.1135+1732C>A
NM_000246.4:c.1052C>A MANE Select	NP_000237.2:p.Ala351Asp
NM_001379330.1:c.908C>A	NP_001366259.1:p.Ala303Asp
NM_001379331.1:c.905C>A	NP_001366260.1:p.Ala302Asp
NM_001379332.1:c.1055C>A	NP_001366261.1:p.Ala352Asp
NM_001379333.1:c.1052C>A	NP_001366262.1:p.Ala351Asp
NM_001379334.1:c.983C>A	NP_001366263.1:p.Ala328Asp