Canonical Allele Identifier: CA7900474

Gene: CIITA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10909069C>T , CM000678.2:g.10909069C>T	GRCh38
NC_000016.9:g.11002926C>T , CM000678.1:g.11002926C>T	GRCh37
NC_000016.8:g.10910427C>T	NCBI36
NG_009628.1:g.36872C>T , LRG_49:g.36872C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000246.4:c.2698C>T MANE Select	NP_000237.2:p.Gln900Ter
ENST00000324288.14:c.2698C>T MANE Select	ENSP00000316328.8:p.Gln900Ter
NM_000246.3:c.2698C>T , LRG_49t1:c.2698C>T	NP_000237.2:p.Gln900Ter
NM_001286402.1:c.2701C>T	NP_001273331.1:p.Gln901Ter
NM_001286403.1:c.946C>T	NP_001273332.1:p.Gln316Ter
NM_001286403.2:c.946C>T	NP_001273332.1:p.Gln316Ter
NM_001379330.1:c.2554C>T	NP_001366259.1:p.Gln852Ter
NM_001379331.1:c.2551C>T	NP_001366260.1:p.Gln851Ter
NM_001379332.1:c.2701C>T	NP_001366261.1:p.Gln901Ter
NM_001379333.1:c.2698C>T	NP_001366262.1:p.Gln900Ter
NM_001379334.1:c.2629C>T	NP_001366263.1:p.Gln877Ter
NR_104444.1:n.1140-1119C>T
NR_104444.2:n.1136-1119C>T
ENST00000324288.12:c.2698C>T	ENSP00000316328.8:p.Gln900Ter
ENST00000381835.9:c.946C>T	ENSP00000371257.5:p.Gln316Ter
ENST00000537380.1:n.1007-1119C>T
ENST00000570546.5:n.3698C>T
ENST00000618207.4:c.1007-1119C>T	ENSP00000484761.1:n.1007-1119C>T
ENST00000618327.4:c.2701C>T	ENSP00000485010.1:p.Gln901Ter
XM_006720880.2:c.2995C>T	XP_006720943.2:p.Gln999Ter
XM_006720880.3:c.2995C>T	XP_006720943.2:p.Gln999Ter
XM_011522484.1:c.2995C>T	XP_011520786.1:p.Gln999Ter
XM_011522484.3:c.2995C>T	XP_011520786.1:p.Gln999Ter
XM_011522485.1:c.2995C>T	XP_011520787.1:p.Gln999Ter
XM_011522485.2:c.2995C>T	XP_011520787.1:p.Gln999Ter
XM_011522486.1:c.2995C>T	XP_011520788.1:p.Gln999Ter
XM_011522486.2:c.2995C>T	XP_011520788.1:p.Gln999Ter
XM_011522487.1:c.2749C>T	XP_011520789.1:p.Gln917Ter
XM_011522487.2:c.2749C>T	XP_011520789.1:p.Gln917Ter
XM_011522488.1:c.2746C>T	XP_011520790.1:p.Gln916Ter
XM_011522488.2:c.2746C>T	XP_011520790.1:p.Gln916Ter
XM_011522489.1:c.2746C>T	XP_011520791.1:p.Gln916Ter
XM_011522489.2:c.2746C>T	XP_011520791.1:p.Gln916Ter
XM_011522490.1:c.2743C>T	XP_011520792.1:p.Gln915Ter
XM_011522490.2:c.2743C>T	XP_011520792.1:p.Gln915Ter
XM_011522491.1:c.2995C>T	XP_011520793.1:p.Gln999Ter
XM_011522491.2:c.2995C>T	XP_011520793.1:p.Gln999Ter
XM_011522492.1:c.2701C>T	XP_011520794.1:p.Gln901Ter
XM_011522492.2:c.2701C>T	XP_011520794.1:p.Gln901Ter
XM_011522493.1:c.2698C>T	XP_011520795.1:p.Gln900Ter
XM_011522493.2:c.2698C>T	XP_011520795.1:p.Gln900Ter
XM_011522494.1:c.2629C>T	XP_011520796.1:p.Gln877Ter
XM_011522494.2:c.2629C>T	XP_011520796.1:p.Gln877Ter
XM_011522495.1:c.2554C>T	XP_011520797.1:p.Gln852Ter
XM_011522495.2:c.2554C>T	XP_011520797.1:p.Gln852Ter
XM_011522496.1:c.2551C>T	XP_011520798.1:p.Gln851Ter
XM_011522496.2:c.2551C>T	XP_011520798.1:p.Gln851Ter
XM_024450280.1:c.2941C>T	XP_024306048.1:p.Gln981Ter
XM_024450281.1:c.2794C>T	XP_024306049.1:p.Gln932Ter
XR_001751904.1:n.3060C>T
XR_932841.1:n.3010C>T
XR_932841.3:n.3012C>T
XR_932842.1:n.3010C>T
XR_932842.2:n.3012C>T
XR_932843.1:n.3010C>T
XR_932846.1:n.3056C>T
XR_932846.3:n.3060C>T
XR_932847.1:n.3056C>T
XR_932847.3:n.3060C>T
XR_932848.1:n.1096C>T