Canonical Allele Identifier: CA394728209

Gene: CIITA

Linked Data

• MyVariant Identifiers: chr16:g.10995934G>C (hg19) ; chr16:g.10902077G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10902077G>C , CM000678.2:g.10902077G>C	GRCh38
NC_000016.9:g.10995934G>C , CM000678.1:g.10995934G>C	GRCh37
NC_000016.8:g.10903435G>C	NCBI36
NG_009628.1:g.29880G>C , LRG_49:g.29880G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695879.1:n.546G>C
ENST00000324288.14:c.521G>C MANE Select	ENSP00000316328.8:p.Gly174Ala
ENST00000637439.1:c.755G>C	ENSP00000489907.1:p.Gly252Ala
ENST00000324288.12:c.521G>C	ENSP00000316328.8:p.Gly174Ala
ENST00000381835.9:c.481+519G>C	ENSP00000371257.5:n.481+519G>C
ENST00000537380.1:n.521G>C
ENST00000570546.5:n.642G>C
ENST00000571186.5:c.*242G>C	ENSP00000459829.1:n.*242G>C
ENST00000573309.5:n.599+519G>C
ENST00000576601.1:c.449G>C	ENSP00000459608.1:p.Gly150Ala
ENST00000611587.4:c.484+519G>C	ENSP00000483487.1:n.484+519G>C
ENST00000618207.4:c.521G>C	ENSP00000484761.1:p.Gly174Ala
ENST00000618327.4:c.524G>C	ENSP00000485010.1:p.Gly175Ala
NM_000246.3:c.521G>C , LRG_49t1:c.521G>C	NP_000237.2:p.Gly174Ala
NM_001286402.1:c.524G>C	NP_001273331.1:p.Gly175Ala
NM_001286403.1:c.481+519G>C	NP_001273332.1:n.481+519G>C
NR_104444.1:n.654G>C
XM_006720880.2:c.818G>C	XP_006720943.2:p.Gly273Ala
XM_011522484.1:c.818G>C	XP_011520786.1:p.Gly273Ala
XM_011522485.1:c.818G>C	XP_011520787.1:p.Gly273Ala
XM_011522486.1:c.818G>C	XP_011520788.1:p.Gly273Ala
XM_011522487.1:c.679+519G>C	XP_011520789.1:n.679+519G>C
XM_011522488.1:c.569G>C	XP_011520790.1:p.Gly190Ala
XM_011522489.1:c.676+519G>C	XP_011520791.1:n.676+519G>C
XM_011522490.1:c.566G>C	XP_011520792.1:p.Gly189Ala
XM_011522491.1:c.818G>C	XP_011520793.1:p.Gly273Ala
XM_011522492.1:c.524G>C	XP_011520794.1:p.Gly175Ala
XM_011522493.1:c.521G>C	XP_011520795.1:p.Gly174Ala
XM_011522494.1:c.452G>C	XP_011520796.1:p.Gly151Ala
XM_011522495.1:c.484+519G>C	XP_011520797.1:n.484+519G>C
XM_011522496.1:c.481+519G>C	XP_011520798.1:n.481+519G>C
XR_932841.1:n.833G>C
XR_932842.1:n.833G>C
XR_932843.1:n.833G>C
XR_932846.1:n.833G>C
XR_932847.1:n.833G>C
XR_932848.1:n.631+519G>C
XM_006720880.3:c.818G>C	XP_006720943.2:p.Gly273Ala
XM_011522484.3:c.818G>C	XP_011520786.1:p.Gly273Ala
XM_011522485.2:c.818G>C	XP_011520787.1:p.Gly273Ala
XM_011522486.2:c.818G>C	XP_011520788.1:p.Gly273Ala
XM_011522487.2:c.679+519G>C	XP_011520789.1:n.679+519G>C
XM_011522488.2:c.569G>C	XP_011520790.1:p.Gly190Ala
XM_011522489.2:c.676+519G>C	XP_011520791.1:n.676+519G>C
XM_011522490.2:c.566G>C	XP_011520792.1:p.Gly189Ala
XM_011522491.2:c.818G>C	XP_011520793.1:p.Gly273Ala
XM_011522492.2:c.524G>C	XP_011520794.1:p.Gly175Ala
XM_011522493.2:c.521G>C	XP_011520795.1:p.Gly174Ala
XM_011522494.2:c.452G>C	XP_011520796.1:p.Gly151Ala
XM_011522495.2:c.484+519G>C	XP_011520797.1:n.484+519G>C
XM_011522496.2:c.481+519G>C	XP_011520798.1:n.481+519G>C
XM_024450280.1:c.764G>C	XP_024306048.1:p.Gly255Ala
XM_024450281.1:c.724+519G>C	XP_024306049.1:n.724+519G>C
XR_001751904.1:n.837G>C
XR_932841.3:n.835G>C
XR_932842.2:n.835G>C
XR_932846.3:n.837G>C
XR_932847.3:n.837G>C
NM_001286403.2:c.481+519G>C	NP_001273332.1:n.481+519G>C
NR_104444.2:n.650G>C
NM_000246.4:c.521G>C MANE Select	NP_000237.2:p.Gly174Ala
NM_001379330.1:c.484+519G>C	NP_001366259.1:n.484+519G>C
NM_001379331.1:c.481+519G>C	NP_001366260.1:n.481+519G>C
NM_001379332.1:c.524G>C	NP_001366261.1:p.Gly175Ala
NM_001379333.1:c.521G>C	NP_001366262.1:p.Gly174Ala
NM_001379334.1:c.452G>C	NP_001366263.1:p.Gly151Ala