Canonical Allele Identifier: CA394728154

Gene: CIITA

Linked Data

• dbSNP Id: rs886051637
• gnomAD v3: 16-10902047-C-A
• gnomAD v4: 16-10902047-C-A
• MyVariant Identifiers: chr16:g.10995904C>A (hg19) ; chr16:g.10902047C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10902047C>A , CM000678.2:g.10902047C>A	GRCh38
NC_000016.9:g.10995904C>A , CM000678.1:g.10995904C>A	GRCh37
NC_000016.8:g.10903405C>A	NCBI36
NG_009628.1:g.29850C>A , LRG_49:g.29850C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695879.1:n.516C>A
ENST00000324288.14:c.491C>A MANE Select	ENSP00000316328.8:p.Pro164His
ENST00000637439.1:c.725C>A	ENSP00000489907.1:p.Pro242His
ENST00000324288.12:c.491C>A	ENSP00000316328.8:p.Pro164His
ENST00000381835.9:c.481+489C>A	ENSP00000371257.5:n.481+489C>A
ENST00000537380.1:n.491C>A
ENST00000570546.5:n.612C>A
ENST00000571186.5:c.*212C>A	ENSP00000459829.1:n.*212C>A
ENST00000573309.5:n.599+489C>A
ENST00000576601.1:c.419C>A	ENSP00000459608.1:p.Pro140His
ENST00000611587.4:c.484+489C>A	ENSP00000483487.1:n.484+489C>A
ENST00000618207.4:c.491C>A	ENSP00000484761.1:p.Pro164His
ENST00000618327.4:c.494C>A	ENSP00000485010.1:p.Pro165His
NM_000246.3:c.491C>A , LRG_49t1:c.491C>A	NP_000237.2:p.Pro164His
NM_001286402.1:c.494C>A	NP_001273331.1:p.Pro165His
NM_001286403.1:c.481+489C>A	NP_001273332.1:n.481+489C>A
NR_104444.1:n.624C>A
XM_006720880.2:c.788C>A	XP_006720943.2:p.Pro263His
XM_011522484.1:c.788C>A	XP_011520786.1:p.Pro263His
XM_011522485.1:c.788C>A	XP_011520787.1:p.Pro263His
XM_011522486.1:c.788C>A	XP_011520788.1:p.Pro263His
XM_011522487.1:c.679+489C>A	XP_011520789.1:n.679+489C>A
XM_011522488.1:c.539C>A	XP_011520790.1:p.Pro180His
XM_011522489.1:c.676+489C>A	XP_011520791.1:n.676+489C>A
XM_011522490.1:c.536C>A	XP_011520792.1:p.Pro179His
XM_011522491.1:c.788C>A	XP_011520793.1:p.Pro263His
XM_011522492.1:c.494C>A	XP_011520794.1:p.Pro165His
XM_011522493.1:c.491C>A	XP_011520795.1:p.Pro164His
XM_011522494.1:c.422C>A	XP_011520796.1:p.Pro141His
XM_011522495.1:c.484+489C>A	XP_011520797.1:n.484+489C>A
XM_011522496.1:c.481+489C>A	XP_011520798.1:n.481+489C>A
XR_932841.1:n.803C>A
XR_932842.1:n.803C>A
XR_932843.1:n.803C>A
XR_932846.1:n.803C>A
XR_932847.1:n.803C>A
XR_932848.1:n.631+489C>A
XM_006720880.3:c.788C>A	XP_006720943.2:p.Pro263His
XM_011522484.3:c.788C>A	XP_011520786.1:p.Pro263His
XM_011522485.2:c.788C>A	XP_011520787.1:p.Pro263His
XM_011522486.2:c.788C>A	XP_011520788.1:p.Pro263His
XM_011522487.2:c.679+489C>A	XP_011520789.1:n.679+489C>A
XM_011522488.2:c.539C>A	XP_011520790.1:p.Pro180His
XM_011522489.2:c.676+489C>A	XP_011520791.1:n.676+489C>A
XM_011522490.2:c.536C>A	XP_011520792.1:p.Pro179His
XM_011522491.2:c.788C>A	XP_011520793.1:p.Pro263His
XM_011522492.2:c.494C>A	XP_011520794.1:p.Pro165His
XM_011522493.2:c.491C>A	XP_011520795.1:p.Pro164His
XM_011522494.2:c.422C>A	XP_011520796.1:p.Pro141His
XM_011522495.2:c.484+489C>A	XP_011520797.1:n.484+489C>A
XM_011522496.2:c.481+489C>A	XP_011520798.1:n.481+489C>A
XM_024450280.1:c.734C>A	XP_024306048.1:p.Pro245His
XM_024450281.1:c.724+489C>A	XP_024306049.1:n.724+489C>A
XR_001751904.1:n.807C>A
XR_932841.3:n.805C>A
XR_932842.2:n.805C>A
XR_932846.3:n.807C>A
XR_932847.3:n.807C>A
NM_001286403.2:c.481+489C>A	NP_001273332.1:n.481+489C>A
NR_104444.2:n.620C>A
NM_000246.4:c.491C>A MANE Select	NP_000237.2:p.Pro164His
NM_001379330.1:c.484+489C>A	NP_001366259.1:n.484+489C>A
NM_001379331.1:c.481+489C>A	NP_001366260.1:n.481+489C>A
NM_001379332.1:c.494C>A	NP_001366261.1:p.Pro165His
NM_001379333.1:c.491C>A	NP_001366262.1:p.Pro164His
NM_001379334.1:c.422C>A	NP_001366263.1:p.Pro141His