Canonical Allele Identifier: CA394734679

Gene: CIITA

Linked Data

• MyVariant Identifiers: chr16:g.11002896A>G (hg19) ; chr16:g.10909039A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10909039A>G , CM000678.2:g.10909039A>G	GRCh38
NC_000016.9:g.11002896A>G , CM000678.1:g.11002896A>G	GRCh37
NC_000016.8:g.10910397A>G	NCBI36
NG_009628.1:g.36842A>G , LRG_49:g.36842A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324288.14:c.2668A>G MANE Select	ENSP00000316328.8:p.Ser890Gly
ENST00000324288.12:c.2668A>G	ENSP00000316328.8:p.Ser890Gly
ENST00000381835.9:c.916A>G	ENSP00000371257.5:p.Ser306Gly
ENST00000537380.1:n.1007-1149A>G
ENST00000570546.5:n.3668A>G
ENST00000618207.4:c.1007-1149A>G	ENSP00000484761.1:n.1007-1149A>G
ENST00000618327.4:c.2671A>G	ENSP00000485010.1:p.Ser891Gly
NM_000246.3:c.2668A>G , LRG_49t1:c.2668A>G	NP_000237.2:p.Ser890Gly
NM_001286402.1:c.2671A>G	NP_001273331.1:p.Ser891Gly
NM_001286403.1:c.916A>G	NP_001273332.1:p.Ser306Gly
NR_104444.1:n.1140-1149A>G
XM_006720880.2:c.2965A>G	XP_006720943.2:p.Ser989Gly
XM_011522484.1:c.2965A>G	XP_011520786.1:p.Ser989Gly
XM_011522485.1:c.2965A>G	XP_011520787.1:p.Ser989Gly
XM_011522486.1:c.2965A>G	XP_011520788.1:p.Ser989Gly
XM_011522487.1:c.2719A>G	XP_011520789.1:p.Ser907Gly
XM_011522488.1:c.2716A>G	XP_011520790.1:p.Ser906Gly
XM_011522489.1:c.2716A>G	XP_011520791.1:p.Ser906Gly
XM_011522490.1:c.2713A>G	XP_011520792.1:p.Ser905Gly
XM_011522491.1:c.2965A>G	XP_011520793.1:p.Ser989Gly
XM_011522492.1:c.2671A>G	XP_011520794.1:p.Ser891Gly
XM_011522493.1:c.2668A>G	XP_011520795.1:p.Ser890Gly
XM_011522494.1:c.2599A>G	XP_011520796.1:p.Ser867Gly
XM_011522495.1:c.2524A>G	XP_011520797.1:p.Ser842Gly
XM_011522496.1:c.2521A>G	XP_011520798.1:p.Ser841Gly
XR_932841.1:n.2980A>G
XR_932842.1:n.2980A>G
XR_932843.1:n.2980A>G
XR_932846.1:n.3026A>G
XR_932847.1:n.3026A>G
XR_932848.1:n.1066A>G
XM_006720880.3:c.2965A>G	XP_006720943.2:p.Ser989Gly
XM_011522484.3:c.2965A>G	XP_011520786.1:p.Ser989Gly
XM_011522485.2:c.2965A>G	XP_011520787.1:p.Ser989Gly
XM_011522486.2:c.2965A>G	XP_011520788.1:p.Ser989Gly
XM_011522487.2:c.2719A>G	XP_011520789.1:p.Ser907Gly
XM_011522488.2:c.2716A>G	XP_011520790.1:p.Ser906Gly
XM_011522489.2:c.2716A>G	XP_011520791.1:p.Ser906Gly
XM_011522490.2:c.2713A>G	XP_011520792.1:p.Ser905Gly
XM_011522491.2:c.2965A>G	XP_011520793.1:p.Ser989Gly
XM_011522492.2:c.2671A>G	XP_011520794.1:p.Ser891Gly
XM_011522493.2:c.2668A>G	XP_011520795.1:p.Ser890Gly
XM_011522494.2:c.2599A>G	XP_011520796.1:p.Ser867Gly
XM_011522495.2:c.2524A>G	XP_011520797.1:p.Ser842Gly
XM_011522496.2:c.2521A>G	XP_011520798.1:p.Ser841Gly
XM_024450280.1:c.2911A>G	XP_024306048.1:p.Ser971Gly
XM_024450281.1:c.2764A>G	XP_024306049.1:p.Ser922Gly
XR_001751904.1:n.3030A>G
XR_932841.3:n.2982A>G
XR_932842.2:n.2982A>G
XR_932846.3:n.3030A>G
XR_932847.3:n.3030A>G
NM_001286403.2:c.916A>G	NP_001273332.1:p.Ser306Gly
NR_104444.2:n.1136-1149A>G
NM_000246.4:c.2668A>G MANE Select	NP_000237.2:p.Ser890Gly
NM_001379330.1:c.2524A>G	NP_001366259.1:p.Ser842Gly
NM_001379331.1:c.2521A>G	NP_001366260.1:p.Ser841Gly
NM_001379332.1:c.2671A>G	NP_001366261.1:p.Ser891Gly
NM_001379333.1:c.2668A>G	NP_001366262.1:p.Ser890Gly
NM_001379334.1:c.2599A>G	NP_001366263.1:p.Ser867Gly