Canonical Allele Identifier: CA394728142

Gene: CIITA

Linked Data

• gnomAD v4: 16-10902041-A-G
• MyVariant Identifiers: chr16:g.10995898A>G (hg19) ; chr16:g.10902041A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10902041A>G , CM000678.2:g.10902041A>G	GRCh38
NC_000016.9:g.10995898A>G , CM000678.1:g.10995898A>G	GRCh37
NC_000016.8:g.10903399A>G	NCBI36
NG_009628.1:g.29844A>G , LRG_49:g.29844A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695879.1:n.510A>G
ENST00000324288.14:c.485A>G MANE Select	ENSP00000316328.8:p.Glu162Gly
ENST00000637439.1:c.719A>G	ENSP00000489907.1:p.Glu240Gly
ENST00000324288.12:c.485A>G	ENSP00000316328.8:p.Glu162Gly
ENST00000381835.9:c.481+483A>G	ENSP00000371257.5:n.481+483A>G
ENST00000537380.1:n.485A>G
ENST00000570546.5:n.606A>G
ENST00000571186.5:c.*206A>G	ENSP00000459829.1:n.*206A>G
ENST00000573309.5:n.599+483A>G
ENST00000576601.1:c.413A>G	ENSP00000459608.1:p.Glu138Gly
ENST00000611587.4:c.484+483A>G	ENSP00000483487.1:n.484+483A>G
ENST00000618207.4:c.485A>G	ENSP00000484761.1:p.Glu162Gly
ENST00000618327.4:c.488A>G	ENSP00000485010.1:p.Glu163Gly
NM_000246.3:c.485A>G , LRG_49t1:c.485A>G	NP_000237.2:p.Glu162Gly
NM_001286402.1:c.488A>G	NP_001273331.1:p.Glu163Gly
NM_001286403.1:c.481+483A>G	NP_001273332.1:n.481+483A>G
NR_104444.1:n.618A>G
XM_006720880.2:c.782A>G	XP_006720943.2:p.Glu261Gly
XM_011522484.1:c.782A>G	XP_011520786.1:p.Glu261Gly
XM_011522485.1:c.782A>G	XP_011520787.1:p.Glu261Gly
XM_011522486.1:c.782A>G	XP_011520788.1:p.Glu261Gly
XM_011522487.1:c.679+483A>G	XP_011520789.1:n.679+483A>G
XM_011522488.1:c.533A>G	XP_011520790.1:p.Glu178Gly
XM_011522489.1:c.676+483A>G	XP_011520791.1:n.676+483A>G
XM_011522490.1:c.530A>G	XP_011520792.1:p.Glu177Gly
XM_011522491.1:c.782A>G	XP_011520793.1:p.Glu261Gly
XM_011522492.1:c.488A>G	XP_011520794.1:p.Glu163Gly
XM_011522493.1:c.485A>G	XP_011520795.1:p.Glu162Gly
XM_011522494.1:c.416A>G	XP_011520796.1:p.Glu139Gly
XM_011522495.1:c.484+483A>G	XP_011520797.1:n.484+483A>G
XM_011522496.1:c.481+483A>G	XP_011520798.1:n.481+483A>G
XR_932841.1:n.797A>G
XR_932842.1:n.797A>G
XR_932843.1:n.797A>G
XR_932846.1:n.797A>G
XR_932847.1:n.797A>G
XR_932848.1:n.631+483A>G
XM_006720880.3:c.782A>G	XP_006720943.2:p.Glu261Gly
XM_011522484.3:c.782A>G	XP_011520786.1:p.Glu261Gly
XM_011522485.2:c.782A>G	XP_011520787.1:p.Glu261Gly
XM_011522486.2:c.782A>G	XP_011520788.1:p.Glu261Gly
XM_011522487.2:c.679+483A>G	XP_011520789.1:n.679+483A>G
XM_011522488.2:c.533A>G	XP_011520790.1:p.Glu178Gly
XM_011522489.2:c.676+483A>G	XP_011520791.1:n.676+483A>G
XM_011522490.2:c.530A>G	XP_011520792.1:p.Glu177Gly
XM_011522491.2:c.782A>G	XP_011520793.1:p.Glu261Gly
XM_011522492.2:c.488A>G	XP_011520794.1:p.Glu163Gly
XM_011522493.2:c.485A>G	XP_011520795.1:p.Glu162Gly
XM_011522494.2:c.416A>G	XP_011520796.1:p.Glu139Gly
XM_011522495.2:c.484+483A>G	XP_011520797.1:n.484+483A>G
XM_011522496.2:c.481+483A>G	XP_011520798.1:n.481+483A>G
XM_024450280.1:c.728A>G	XP_024306048.1:p.Glu243Gly
XM_024450281.1:c.724+483A>G	XP_024306049.1:n.724+483A>G
XR_001751904.1:n.801A>G
XR_932841.3:n.799A>G
XR_932842.2:n.799A>G
XR_932846.3:n.801A>G
XR_932847.3:n.801A>G
NM_001286403.2:c.481+483A>G	NP_001273332.1:n.481+483A>G
NR_104444.2:n.614A>G
NM_000246.4:c.485A>G MANE Select	NP_000237.2:p.Glu162Gly
NM_001379330.1:c.484+483A>G	NP_001366259.1:n.484+483A>G
NM_001379331.1:c.481+483A>G	NP_001366260.1:n.481+483A>G
NM_001379332.1:c.488A>G	NP_001366261.1:p.Glu163Gly
NM_001379333.1:c.485A>G	NP_001366262.1:p.Glu162Gly
NM_001379334.1:c.416A>G	NP_001366263.1:p.Glu139Gly