Canonical Allele Identifier: CA394734699

Gene: CIITA

Linked Data

• MyVariant Identifiers: chr16:g.11002901C>G (hg19) ; chr16:g.10909044C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10909044C>G , CM000678.2:g.10909044C>G	GRCh38
NC_000016.9:g.11002901C>G , CM000678.1:g.11002901C>G	GRCh37
NC_000016.8:g.10910402C>G	NCBI36
NG_009628.1:g.36847C>G , LRG_49:g.36847C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324288.14:c.2673C>G MANE Select	ENSP00000316328.8:p.Asp891Glu
ENST00000324288.12:c.2673C>G	ENSP00000316328.8:p.Asp891Glu
ENST00000381835.9:c.921C>G	ENSP00000371257.5:p.Asp307Glu
ENST00000537380.1:n.1007-1144C>G
ENST00000570546.5:n.3673C>G
ENST00000618207.4:c.1007-1144C>G	ENSP00000484761.1:n.1007-1144C>G
ENST00000618327.4:c.2676C>G	ENSP00000485010.1:p.Asp892Glu
NM_000246.3:c.2673C>G , LRG_49t1:c.2673C>G	NP_000237.2:p.Asp891Glu
NM_001286402.1:c.2676C>G	NP_001273331.1:p.Asp892Glu
NM_001286403.1:c.921C>G	NP_001273332.1:p.Asp307Glu
NR_104444.1:n.1140-1144C>G
XM_006720880.2:c.2970C>G	XP_006720943.2:p.Asp990Glu
XM_011522484.1:c.2970C>G	XP_011520786.1:p.Asp990Glu
XM_011522485.1:c.2970C>G	XP_011520787.1:p.Asp990Glu
XM_011522486.1:c.2970C>G	XP_011520788.1:p.Asp990Glu
XM_011522487.1:c.2724C>G	XP_011520789.1:p.Asp908Glu
XM_011522488.1:c.2721C>G	XP_011520790.1:p.Asp907Glu
XM_011522489.1:c.2721C>G	XP_011520791.1:p.Asp907Glu
XM_011522490.1:c.2718C>G	XP_011520792.1:p.Asp906Glu
XM_011522491.1:c.2970C>G	XP_011520793.1:p.Asp990Glu
XM_011522492.1:c.2676C>G	XP_011520794.1:p.Asp892Glu
XM_011522493.1:c.2673C>G	XP_011520795.1:p.Asp891Glu
XM_011522494.1:c.2604C>G	XP_011520796.1:p.Asp868Glu
XM_011522495.1:c.2529C>G	XP_011520797.1:p.Asp843Glu
XM_011522496.1:c.2526C>G	XP_011520798.1:p.Asp842Glu
XR_932841.1:n.2985C>G
XR_932842.1:n.2985C>G
XR_932843.1:n.2985C>G
XR_932846.1:n.3031C>G
XR_932847.1:n.3031C>G
XR_932848.1:n.1071C>G
XM_006720880.3:c.2970C>G	XP_006720943.2:p.Asp990Glu
XM_011522484.3:c.2970C>G	XP_011520786.1:p.Asp990Glu
XM_011522485.2:c.2970C>G	XP_011520787.1:p.Asp990Glu
XM_011522486.2:c.2970C>G	XP_011520788.1:p.Asp990Glu
XM_011522487.2:c.2724C>G	XP_011520789.1:p.Asp908Glu
XM_011522488.2:c.2721C>G	XP_011520790.1:p.Asp907Glu
XM_011522489.2:c.2721C>G	XP_011520791.1:p.Asp907Glu
XM_011522490.2:c.2718C>G	XP_011520792.1:p.Asp906Glu
XM_011522491.2:c.2970C>G	XP_011520793.1:p.Asp990Glu
XM_011522492.2:c.2676C>G	XP_011520794.1:p.Asp892Glu
XM_011522493.2:c.2673C>G	XP_011520795.1:p.Asp891Glu
XM_011522494.2:c.2604C>G	XP_011520796.1:p.Asp868Glu
XM_011522495.2:c.2529C>G	XP_011520797.1:p.Asp843Glu
XM_011522496.2:c.2526C>G	XP_011520798.1:p.Asp842Glu
XM_024450280.1:c.2916C>G	XP_024306048.1:p.Asp972Glu
XM_024450281.1:c.2769C>G	XP_024306049.1:p.Asp923Glu
XR_001751904.1:n.3035C>G
XR_932841.3:n.2987C>G
XR_932842.2:n.2987C>G
XR_932846.3:n.3035C>G
XR_932847.3:n.3035C>G
NM_001286403.2:c.921C>G	NP_001273332.1:p.Asp307Glu
NR_104444.2:n.1136-1144C>G
NM_000246.4:c.2673C>G MANE Select	NP_000237.2:p.Asp891Glu
NM_001379330.1:c.2529C>G	NP_001366259.1:p.Asp843Glu
NM_001379331.1:c.2526C>G	NP_001366260.1:p.Asp842Glu
NM_001379332.1:c.2676C>G	NP_001366261.1:p.Asp892Glu
NM_001379333.1:c.2673C>G	NP_001366262.1:p.Asp891Glu
NM_001379334.1:c.2604C>G	NP_001366263.1:p.Asp868Glu