Canonical Allele Identifier: CA7899947
Community Standard Title: NM_000246.4(CIITA):c.931A>G (p.Met311Val)
Gene: CIITA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.10903889A>G , CM000678.2:g.10903889A>G GRCh38
NC_000016.9:g.10997746A>G , CM000678.1:g.10997746A>G GRCh37
NC_000016.8:g.10905247A>G NCBI36
NG_009628.1:g.31692A>G , LRG_49:g.31692A>G

Transcript Alleles

HGVS Amino-acid Change
NM_000246.4:c.931A>G MANE Select NP_000237.2:p.Met311Val
ENST00000324288.14:c.931A>G MANE Select ENSP00000316328.8:p.Met311Val
NM_000246.3:c.931A>G , LRG_49t1:c.931A>G NP_000237.2:p.Met311Val
NM_001286402.1:c.934A>G NP_001273331.1:p.Met312Val
NM_001286403.1:c.784A>G NP_001273332.1:p.Met262Val
NM_001286403.2:c.784A>G NP_001273332.1:p.Met262Val
NM_001379330.1:c.787A>G NP_001366259.1:p.Met263Val
NM_001379331.1:c.784A>G NP_001366260.1:p.Met262Val
NM_001379332.1:c.934A>G NP_001366261.1:p.Met312Val
NM_001379333.1:c.931A>G NP_001366262.1:p.Met311Val
NM_001379334.1:c.862A>G NP_001366263.1:p.Met288Val
NR_104444.1:n.1064A>G
NR_104444.2:n.1060A>G
ENST00000324288.12:c.931A>G ENSP00000316328.8:p.Met311Val
ENST00000381835.9:c.784A>G ENSP00000371257.5:p.Met262Val
ENST00000537380.1:n.931A>G
ENST00000570546.5:n.1052A>G
ENST00000573309.5:n.902A>G
ENST00000611587.4:c.787A>G ENSP00000483487.1:p.Met263Val
ENST00000618207.4:c.931A>G ENSP00000484761.1:p.Met311Val
ENST00000618327.4:c.934A>G ENSP00000485010.1:p.Met312Val
ENST00000695879.1:n.956A>G
XM_006720880.2:c.1228A>G XP_006720943.2:p.Met410Val
XM_006720880.3:c.1228A>G XP_006720943.2:p.Met410Val
XM_011522484.1:c.1228A>G XP_011520786.1:p.Met410Val
XM_011522484.3:c.1228A>G XP_011520786.1:p.Met410Val
XM_011522485.1:c.1228A>G XP_011520787.1:p.Met410Val
XM_011522485.2:c.1228A>G XP_011520787.1:p.Met410Val
XM_011522486.1:c.1228A>G XP_011520788.1:p.Met410Val
XM_011522486.2:c.1228A>G XP_011520788.1:p.Met410Val
XM_011522487.1:c.982A>G XP_011520789.1:p.Met328Val
XM_011522487.2:c.982A>G XP_011520789.1:p.Met328Val
XM_011522488.1:c.979A>G XP_011520790.1:p.Met327Val
XM_011522488.2:c.979A>G XP_011520790.1:p.Met327Val
XM_011522489.1:c.979A>G XP_011520791.1:p.Met327Val
XM_011522489.2:c.979A>G XP_011520791.1:p.Met327Val
XM_011522490.1:c.976A>G XP_011520792.1:p.Met326Val
XM_011522490.2:c.976A>G XP_011520792.1:p.Met326Val
XM_011522491.1:c.1228A>G XP_011520793.1:p.Met410Val
XM_011522491.2:c.1228A>G XP_011520793.1:p.Met410Val
XM_011522492.1:c.934A>G XP_011520794.1:p.Met312Val
XM_011522492.2:c.934A>G XP_011520794.1:p.Met312Val
XM_011522493.1:c.931A>G XP_011520795.1:p.Met311Val
XM_011522493.2:c.931A>G XP_011520795.1:p.Met311Val
XM_011522494.1:c.862A>G XP_011520796.1:p.Met288Val
XM_011522494.2:c.862A>G XP_011520796.1:p.Met288Val
XM_011522495.1:c.787A>G XP_011520797.1:p.Met263Val
XM_011522495.2:c.787A>G XP_011520797.1:p.Met263Val
XM_011522496.1:c.784A>G XP_011520798.1:p.Met262Val
XM_011522496.2:c.784A>G XP_011520798.1:p.Met262Val
XM_024450280.1:c.1174A>G XP_024306048.1:p.Met392Val
XM_024450281.1:c.1027A>G XP_024306049.1:p.Met343Val
XR_001751904.1:n.1247A>G
XR_932841.1:n.1243A>G
XR_932841.3:n.1245A>G
XR_932842.1:n.1243A>G
XR_932842.2:n.1245A>G
XR_932843.1:n.1243A>G
XR_932846.1:n.1243A>G
XR_932846.3:n.1247A>G
XR_932847.1:n.1243A>G
XR_932847.3:n.1247A>G
XR_932848.1:n.934A>G