Canonical Allele Identifier: CA394731242

Gene: CIITA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10907107C>T , CM000678.2:g.10907107C>T	GRCh38
NC_000016.9:g.11000964C>T , CM000678.1:g.11000964C>T	GRCh37
NC_000016.8:g.10908465C>T	NCBI36
NG_009628.1:g.34910C>T , LRG_49:g.34910C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000246.4:c.1615C>T MANE Select	NP_000237.2:p.Arg539Ter
ENST00000324288.14:c.1615C>T MANE Select	ENSP00000316328.8:p.Arg539Ter
NM_000246.3:c.1615C>T , LRG_49t1:c.1615C>T	NP_000237.2:p.Arg539Ter
NM_001286402.1:c.1618C>T	NP_001273331.1:p.Arg540Ter
NM_001286403.1:c.860-1876C>T	NP_001273332.1:n.860-1876C>T
NM_001286403.2:c.860-1876C>T	NP_001273332.1:n.860-1876C>T
NM_001379330.1:c.1471C>T	NP_001366259.1:p.Arg491Ter
NM_001379331.1:c.1468C>T	NP_001366260.1:p.Arg490Ter
NM_001379332.1:c.1618C>T	NP_001366261.1:p.Arg540Ter
NM_001379333.1:c.1615C>T	NP_001366262.1:p.Arg539Ter
NM_001379334.1:c.1546C>T	NP_001366263.1:p.Arg516Ter
NR_104444.1:n.1139+2295C>T
NR_104444.2:n.1135+2295C>T
ENST00000324288.12:c.1615C>T	ENSP00000316328.8:p.Arg539Ter
ENST00000381835.9:c.860-1876C>T	ENSP00000371257.5:n.860-1876C>T
ENST00000537380.1:n.1006+2295C>T
ENST00000570546.5:n.1736C>T
ENST00000573309.5:n.1586C>T
ENST00000611587.4:c.1471C>T	ENSP00000483487.1:p.Arg491Ter
ENST00000618207.4:c.1006+2295C>T	ENSP00000484761.1:n.1006+2295C>T
ENST00000618327.4:c.1618C>T	ENSP00000485010.1:p.Arg540Ter
ENST00000695879.1:n.1509C>T
XM_006720880.2:c.1912C>T	XP_006720943.2:p.Arg638Ter
XM_006720880.3:c.1912C>T	XP_006720943.2:p.Arg638Ter
XM_011522484.1:c.1912C>T	XP_011520786.1:p.Arg638Ter
XM_011522484.3:c.1912C>T	XP_011520786.1:p.Arg638Ter
XM_011522485.1:c.1912C>T	XP_011520787.1:p.Arg638Ter
XM_011522485.2:c.1912C>T	XP_011520787.1:p.Arg638Ter
XM_011522486.1:c.1912C>T	XP_011520788.1:p.Arg638Ter
XM_011522486.2:c.1912C>T	XP_011520788.1:p.Arg638Ter
XM_011522487.1:c.1666C>T	XP_011520789.1:p.Arg556Ter
XM_011522487.2:c.1666C>T	XP_011520789.1:p.Arg556Ter
XM_011522488.1:c.1663C>T	XP_011520790.1:p.Arg555Ter
XM_011522488.2:c.1663C>T	XP_011520790.1:p.Arg555Ter
XM_011522489.1:c.1663C>T	XP_011520791.1:p.Arg555Ter
XM_011522489.2:c.1663C>T	XP_011520791.1:p.Arg555Ter
XM_011522490.1:c.1660C>T	XP_011520792.1:p.Arg554Ter
XM_011522490.2:c.1660C>T	XP_011520792.1:p.Arg554Ter
XM_011522491.1:c.1912C>T	XP_011520793.1:p.Arg638Ter
XM_011522491.2:c.1912C>T	XP_011520793.1:p.Arg638Ter
XM_011522492.1:c.1618C>T	XP_011520794.1:p.Arg540Ter
XM_011522492.2:c.1618C>T	XP_011520794.1:p.Arg540Ter
XM_011522493.1:c.1615C>T	XP_011520795.1:p.Arg539Ter
XM_011522493.2:c.1615C>T	XP_011520795.1:p.Arg539Ter
XM_011522494.1:c.1546C>T	XP_011520796.1:p.Arg516Ter
XM_011522494.2:c.1546C>T	XP_011520796.1:p.Arg516Ter
XM_011522495.1:c.1471C>T	XP_011520797.1:p.Arg491Ter
XM_011522495.2:c.1471C>T	XP_011520797.1:p.Arg491Ter
XM_011522496.1:c.1468C>T	XP_011520798.1:p.Arg490Ter
XM_011522496.2:c.1468C>T	XP_011520798.1:p.Arg490Ter
XM_024450280.1:c.1858C>T	XP_024306048.1:p.Arg620Ter
XM_024450281.1:c.1711C>T	XP_024306049.1:p.Arg571Ter
XR_001751904.1:n.1931C>T
XR_932841.1:n.1927C>T
XR_932841.3:n.1929C>T
XR_932842.1:n.1927C>T
XR_932842.2:n.1929C>T
XR_932843.1:n.1927C>T
XR_932846.1:n.1927C>T
XR_932846.3:n.1931C>T
XR_932847.1:n.1927C>T
XR_932847.3:n.1931C>T
XR_932848.1:n.1010-1876C>T