Canonical Allele Identifier: CA394734684

Gene: CIITA

Linked Data

• MyVariant Identifiers: chr16:g.11002897G>C (hg19) ; chr16:g.10909040G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10909040G>C , CM000678.2:g.10909040G>C	GRCh38
NC_000016.9:g.11002897G>C , CM000678.1:g.11002897G>C	GRCh37
NC_000016.8:g.10910398G>C	NCBI36
NG_009628.1:g.36843G>C , LRG_49:g.36843G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324288.14:c.2669G>C MANE Select	ENSP00000316328.8:p.Ser890Thr
ENST00000324288.12:c.2669G>C	ENSP00000316328.8:p.Ser890Thr
ENST00000381835.9:c.917G>C	ENSP00000371257.5:p.Ser306Thr
ENST00000537380.1:n.1007-1148G>C
ENST00000570546.5:n.3669G>C
ENST00000618207.4:c.1007-1148G>C	ENSP00000484761.1:n.1007-1148G>C
ENST00000618327.4:c.2672G>C	ENSP00000485010.1:p.Ser891Thr
NM_000246.3:c.2669G>C , LRG_49t1:c.2669G>C	NP_000237.2:p.Ser890Thr
NM_001286402.1:c.2672G>C	NP_001273331.1:p.Ser891Thr
NM_001286403.1:c.917G>C	NP_001273332.1:p.Ser306Thr
NR_104444.1:n.1140-1148G>C
XM_006720880.2:c.2966G>C	XP_006720943.2:p.Ser989Thr
XM_011522484.1:c.2966G>C	XP_011520786.1:p.Ser989Thr
XM_011522485.1:c.2966G>C	XP_011520787.1:p.Ser989Thr
XM_011522486.1:c.2966G>C	XP_011520788.1:p.Ser989Thr
XM_011522487.1:c.2720G>C	XP_011520789.1:p.Ser907Thr
XM_011522488.1:c.2717G>C	XP_011520790.1:p.Ser906Thr
XM_011522489.1:c.2717G>C	XP_011520791.1:p.Ser906Thr
XM_011522490.1:c.2714G>C	XP_011520792.1:p.Ser905Thr
XM_011522491.1:c.2966G>C	XP_011520793.1:p.Ser989Thr
XM_011522492.1:c.2672G>C	XP_011520794.1:p.Ser891Thr
XM_011522493.1:c.2669G>C	XP_011520795.1:p.Ser890Thr
XM_011522494.1:c.2600G>C	XP_011520796.1:p.Ser867Thr
XM_011522495.1:c.2525G>C	XP_011520797.1:p.Ser842Thr
XM_011522496.1:c.2522G>C	XP_011520798.1:p.Ser841Thr
XR_932841.1:n.2981G>C
XR_932842.1:n.2981G>C
XR_932843.1:n.2981G>C
XR_932846.1:n.3027G>C
XR_932847.1:n.3027G>C
XR_932848.1:n.1067G>C
XM_006720880.3:c.2966G>C	XP_006720943.2:p.Ser989Thr
XM_011522484.3:c.2966G>C	XP_011520786.1:p.Ser989Thr
XM_011522485.2:c.2966G>C	XP_011520787.1:p.Ser989Thr
XM_011522486.2:c.2966G>C	XP_011520788.1:p.Ser989Thr
XM_011522487.2:c.2720G>C	XP_011520789.1:p.Ser907Thr
XM_011522488.2:c.2717G>C	XP_011520790.1:p.Ser906Thr
XM_011522489.2:c.2717G>C	XP_011520791.1:p.Ser906Thr
XM_011522490.2:c.2714G>C	XP_011520792.1:p.Ser905Thr
XM_011522491.2:c.2966G>C	XP_011520793.1:p.Ser989Thr
XM_011522492.2:c.2672G>C	XP_011520794.1:p.Ser891Thr
XM_011522493.2:c.2669G>C	XP_011520795.1:p.Ser890Thr
XM_011522494.2:c.2600G>C	XP_011520796.1:p.Ser867Thr
XM_011522495.2:c.2525G>C	XP_011520797.1:p.Ser842Thr
XM_011522496.2:c.2522G>C	XP_011520798.1:p.Ser841Thr
XM_024450280.1:c.2912G>C	XP_024306048.1:p.Ser971Thr
XM_024450281.1:c.2765G>C	XP_024306049.1:p.Ser922Thr
XR_001751904.1:n.3031G>C
XR_932841.3:n.2983G>C
XR_932842.2:n.2983G>C
XR_932846.3:n.3031G>C
XR_932847.3:n.3031G>C
NM_001286403.2:c.917G>C	NP_001273332.1:p.Ser306Thr
NR_104444.2:n.1136-1148G>C
NM_000246.4:c.2669G>C MANE Select	NP_000237.2:p.Ser890Thr
NM_001379330.1:c.2525G>C	NP_001366259.1:p.Ser842Thr
NM_001379331.1:c.2522G>C	NP_001366260.1:p.Ser841Thr
NM_001379332.1:c.2672G>C	NP_001366261.1:p.Ser891Thr
NM_001379333.1:c.2669G>C	NP_001366262.1:p.Ser890Thr
NM_001379334.1:c.2600G>C	NP_001366263.1:p.Ser867Thr