Canonical Allele Identifier: CA7900751
Community Standard Title: NM_000246.4(CIITA):c.3234C>T (p.Asp1078=)
Gene: CIITA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.10922407C>T , CM000678.2:g.10922407C>T GRCh38
NC_000016.9:g.11016264C>T , CM000678.1:g.11016264C>T GRCh37
NC_000016.8:g.10923765C>T NCBI36
NG_009628.1:g.50210C>T , LRG_49:g.50210C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000246.4:c.3234C>T MANE Select NP_000237.2:p.Asp1078=
ENST00000324288.14:c.3234C>T MANE Select ENSP00000316328.8:p.Asp1078=
NM_000246.3:c.3234C>T , LRG_49t1:c.3234C>T NP_000237.2:p.Asp1078=
NM_001286402.1:c.3237C>T NP_001273331.1:p.Asp1079=
NM_001286403.1:c.1482C>T NP_001273332.1:p.Asp494=
NM_001286403.2:c.1482C>T NP_001273332.1:p.Asp494=
NM_001379330.1:c.3090C>T NP_001366259.1:p.Asp1030=
NM_001379331.1:c.3087C>T NP_001366260.1:p.Asp1029=
NM_001379332.1:c.3237C>T NP_001366261.1:p.Asp1079=
NM_001379333.1:c.3234C>T NP_001366262.1:p.Asp1078=
NM_001379334.1:c.3165C>T NP_001366263.1:p.Asp1055=
NR_104444.1:n.1557C>T
NR_104444.2:n.1553C>T
ENST00000324288.12:c.3234C>T ENSP00000316328.8:p.Asp1078=
ENST00000381835.9:c.1482C>T ENSP00000371257.5:p.Asp494=
ENST00000570546.5:n.4234C>T
ENST00000618207.4:c.*362C>T ENSP00000484761.1:n.*362C>T
ENST00000618327.4:c.3237C>T ENSP00000485010.1:p.Asp1079=
ENST00000644232.1:c.85C>T
ENST00000646979.1:c.85C>T
XM_006720880.2:c.3531C>T XP_006720943.2:p.Asp1177=
XM_006720880.3:c.3531C>T XP_006720943.2:p.Asp1177=
XM_011522484.1:c.3531C>T XP_011520786.1:p.Asp1177=
XM_011522484.3:c.3531C>T XP_011520786.1:p.Asp1177=
XM_011522485.1:c.3531C>T XP_011520787.1:p.Asp1177=
XM_011522485.2:c.3531C>T XP_011520787.1:p.Asp1177=
XM_011522487.1:c.3285C>T XP_011520789.1:p.Asp1095=
XM_011522487.2:c.3285C>T XP_011520789.1:p.Asp1095=
XM_011522488.1:c.3282C>T XP_011520790.1:p.Asp1094=
XM_011522488.2:c.3282C>T XP_011520790.1:p.Asp1094=
XM_011522489.1:c.3282C>T XP_011520791.1:p.Asp1094=
XM_011522489.2:c.3282C>T XP_011520791.1:p.Asp1094=
XM_011522490.1:c.3279C>T XP_011520792.1:p.Asp1093=
XM_011522490.2:c.3279C>T XP_011520792.1:p.Asp1093=
XM_011522492.1:c.3237C>T XP_011520794.1:p.Asp1079=
XM_011522492.2:c.3237C>T XP_011520794.1:p.Asp1079=
XM_011522493.1:c.3234C>T XP_011520795.1:p.Asp1078=
XM_011522493.2:c.3234C>T XP_011520795.1:p.Asp1078=
XM_011522494.1:c.3165C>T XP_011520796.1:p.Asp1055=
XM_011522494.2:c.3165C>T XP_011520796.1:p.Asp1055=
XM_011522495.1:c.3090C>T XP_011520797.1:p.Asp1030=
XM_011522495.2:c.3090C>T XP_011520797.1:p.Asp1030=
XM_011522496.1:c.3087C>T XP_011520798.1:p.Asp1029=
XM_011522496.2:c.3087C>T XP_011520798.1:p.Asp1029=
XM_024450280.1:c.3477C>T XP_024306048.1:p.Asp1159=
XM_024450281.1:c.3330C>T XP_024306049.1:p.Asp1110=
XR_001751904.1:n.3596C>T
XR_932841.1:n.3546C>T
XR_932841.3:n.3548C>T
XR_932842.1:n.3546C>T
XR_932842.2:n.3548C>T
XR_932843.1:n.3546C>T
XR_932846.1:n.3592C>T
XR_932846.3:n.3596C>T
XR_932848.1:n.1632C>T