Canonical Allele Identifier: CA394734704

Gene: CIITA

Linked Data

• dbSNP Id: rs1334030589
• gnomAD v3: 16-10909046-C-T
• gnomAD v4: 16-10909046-C-T
• MyVariant Identifiers: chr16:g.11002903C>T (hg19) ; chr16:g.10909046C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10909046C>T , CM000678.2:g.10909046C>T	GRCh38
NC_000016.9:g.11002903C>T , CM000678.1:g.11002903C>T	GRCh37
NC_000016.8:g.10910404C>T	NCBI36
NG_009628.1:g.36849C>T , LRG_49:g.36849C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324288.14:c.2675C>T MANE Select	ENSP00000316328.8:p.Thr892Met
ENST00000324288.12:c.2675C>T	ENSP00000316328.8:p.Thr892Met
ENST00000381835.9:c.923C>T	ENSP00000371257.5:p.Thr308Met
ENST00000537380.1:n.1007-1142C>T
ENST00000570546.5:n.3675C>T
ENST00000618207.4:c.1007-1142C>T	ENSP00000484761.1:n.1007-1142C>T
ENST00000618327.4:c.2678C>T	ENSP00000485010.1:p.Thr893Met
NM_000246.3:c.2675C>T , LRG_49t1:c.2675C>T	NP_000237.2:p.Thr892Met
NM_001286402.1:c.2678C>T	NP_001273331.1:p.Thr893Met
NM_001286403.1:c.923C>T	NP_001273332.1:p.Thr308Met
NR_104444.1:n.1140-1142C>T
XM_006720880.2:c.2972C>T	XP_006720943.2:p.Thr991Met
XM_011522484.1:c.2972C>T	XP_011520786.1:p.Thr991Met
XM_011522485.1:c.2972C>T	XP_011520787.1:p.Thr991Met
XM_011522486.1:c.2972C>T	XP_011520788.1:p.Thr991Met
XM_011522487.1:c.2726C>T	XP_011520789.1:p.Thr909Met
XM_011522488.1:c.2723C>T	XP_011520790.1:p.Thr908Met
XM_011522489.1:c.2723C>T	XP_011520791.1:p.Thr908Met
XM_011522490.1:c.2720C>T	XP_011520792.1:p.Thr907Met
XM_011522491.1:c.2972C>T	XP_011520793.1:p.Thr991Met
XM_011522492.1:c.2678C>T	XP_011520794.1:p.Thr893Met
XM_011522493.1:c.2675C>T	XP_011520795.1:p.Thr892Met
XM_011522494.1:c.2606C>T	XP_011520796.1:p.Thr869Met
XM_011522495.1:c.2531C>T	XP_011520797.1:p.Thr844Met
XM_011522496.1:c.2528C>T	XP_011520798.1:p.Thr843Met
XR_932841.1:n.2987C>T
XR_932842.1:n.2987C>T
XR_932843.1:n.2987C>T
XR_932846.1:n.3033C>T
XR_932847.1:n.3033C>T
XR_932848.1:n.1073C>T
XM_006720880.3:c.2972C>T	XP_006720943.2:p.Thr991Met
XM_011522484.3:c.2972C>T	XP_011520786.1:p.Thr991Met
XM_011522485.2:c.2972C>T	XP_011520787.1:p.Thr991Met
XM_011522486.2:c.2972C>T	XP_011520788.1:p.Thr991Met
XM_011522487.2:c.2726C>T	XP_011520789.1:p.Thr909Met
XM_011522488.2:c.2723C>T	XP_011520790.1:p.Thr908Met
XM_011522489.2:c.2723C>T	XP_011520791.1:p.Thr908Met
XM_011522490.2:c.2720C>T	XP_011520792.1:p.Thr907Met
XM_011522491.2:c.2972C>T	XP_011520793.1:p.Thr991Met
XM_011522492.2:c.2678C>T	XP_011520794.1:p.Thr893Met
XM_011522493.2:c.2675C>T	XP_011520795.1:p.Thr892Met
XM_011522494.2:c.2606C>T	XP_011520796.1:p.Thr869Met
XM_011522495.2:c.2531C>T	XP_011520797.1:p.Thr844Met
XM_011522496.2:c.2528C>T	XP_011520798.1:p.Thr843Met
XM_024450280.1:c.2918C>T	XP_024306048.1:p.Thr973Met
XM_024450281.1:c.2771C>T	XP_024306049.1:p.Thr924Met
XR_001751904.1:n.3037C>T
XR_932841.3:n.2989C>T
XR_932842.2:n.2989C>T
XR_932846.3:n.3037C>T
XR_932847.3:n.3037C>T
NM_001286403.2:c.923C>T	NP_001273332.1:p.Thr308Met
NR_104444.2:n.1136-1142C>T
NM_000246.4:c.2675C>T MANE Select	NP_000237.2:p.Thr892Met
NM_001379330.1:c.2531C>T	NP_001366259.1:p.Thr844Met
NM_001379331.1:c.2528C>T	NP_001366260.1:p.Thr843Met
NM_001379332.1:c.2678C>T	NP_001366261.1:p.Thr893Met
NM_001379333.1:c.2675C>T	NP_001366262.1:p.Thr892Met
NM_001379334.1:c.2606C>T	NP_001366263.1:p.Thr869Met