Canonical Allele Identifier: CA493695036

Gene: CIITA

Linked Data

• MyVariant Identifiers: chr16:g.11000399T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10906542T>C , CM000678.2:g.10906542T>C	GRCh38
NC_000016.9:g.11000399T>C , CM000678.1:g.11000399T>C	GRCh37
NC_000016.8:g.10907900T>C	NCBI36
NG_009628.1:g.34345T>C , LRG_49:g.34345T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000695879.1:n.1075T>C
ENST00000324288.14:c.1050T>C MANE Select	ENSP00000316328.8:p.Gly350=
ENST00000324288.12:c.1050T>C	ENSP00000316328.8:p.Gly350=
ENST00000381835.9:c.859+1730T>C	ENSP00000371257.5:n.859+1730T>C
ENST00000537380.1:n.1006+1730T>C
ENST00000570546.5:n.1171T>C
ENST00000573309.5:n.1021T>C
ENST00000611587.4:c.906T>C	ENSP00000483487.1:p.Gly302=
ENST00000618207.4:c.1006+1730T>C	ENSP00000484761.1:n.1006+1730T>C
ENST00000618327.4:c.1053T>C	ENSP00000485010.1:p.Gly351=
NM_000246.3:c.1050T>C , LRG_49t1:c.1050T>C	NP_000237.2:p.Gly350=
NM_001286402.1:c.1053T>C	NP_001273331.1:p.Gly351=
NM_001286403.1:c.859+1730T>C	NP_001273332.1:n.859+1730T>C
NR_104444.1:n.1139+1730T>C
XM_006720880.2:c.1347T>C	XP_006720943.2:p.Gly449=
XM_011522484.1:c.1347T>C	XP_011520786.1:p.Gly449=
XM_011522485.1:c.1347T>C	XP_011520787.1:p.Gly449=
XM_011522486.1:c.1347T>C	XP_011520788.1:p.Gly449=
XM_011522487.1:c.1101T>C	XP_011520789.1:p.Gly367=
XM_011522488.1:c.1098T>C	XP_011520790.1:p.Gly366=
XM_011522489.1:c.1098T>C	XP_011520791.1:p.Gly366=
XM_011522490.1:c.1095T>C	XP_011520792.1:p.Gly365=
XM_011522491.1:c.1347T>C	XP_011520793.1:p.Gly449=
XM_011522492.1:c.1053T>C	XP_011520794.1:p.Gly351=
XM_011522493.1:c.1050T>C	XP_011520795.1:p.Gly350=
XM_011522494.1:c.981T>C	XP_011520796.1:p.Gly327=
XM_011522495.1:c.906T>C	XP_011520797.1:p.Gly302=
XM_011522496.1:c.903T>C	XP_011520798.1:p.Gly301=
XR_932841.1:n.1362T>C
XR_932842.1:n.1362T>C
XR_932843.1:n.1362T>C
XR_932846.1:n.1362T>C
XR_932847.1:n.1362T>C
XR_932848.1:n.1009+1730T>C
XM_006720880.3:c.1347T>C	XP_006720943.2:p.Gly449=
XM_011522484.3:c.1347T>C	XP_011520786.1:p.Gly449=
XM_011522485.2:c.1347T>C	XP_011520787.1:p.Gly449=
XM_011522486.2:c.1347T>C	XP_011520788.1:p.Gly449=
XM_011522487.2:c.1101T>C	XP_011520789.1:p.Gly367=
XM_011522488.2:c.1098T>C	XP_011520790.1:p.Gly366=
XM_011522489.2:c.1098T>C	XP_011520791.1:p.Gly366=
XM_011522490.2:c.1095T>C	XP_011520792.1:p.Gly365=
XM_011522491.2:c.1347T>C	XP_011520793.1:p.Gly449=
XM_011522492.2:c.1053T>C	XP_011520794.1:p.Gly351=
XM_011522493.2:c.1050T>C	XP_011520795.1:p.Gly350=
XM_011522494.2:c.981T>C	XP_011520796.1:p.Gly327=
XM_011522495.2:c.906T>C	XP_011520797.1:p.Gly302=
XM_011522496.2:c.903T>C	XP_011520798.1:p.Gly301=
XM_024450280.1:c.1293T>C	XP_024306048.1:p.Gly431=
XM_024450281.1:c.1146T>C	XP_024306049.1:p.Gly382=
XR_001751904.1:n.1366T>C
XR_932841.3:n.1364T>C
XR_932842.2:n.1364T>C
XR_932846.3:n.1366T>C
XR_932847.3:n.1366T>C
NM_001286403.2:c.859+1730T>C	NP_001273332.1:n.859+1730T>C
NR_104444.2:n.1135+1730T>C
NM_000246.4:c.1050T>C MANE Select	NP_000237.2:p.Gly350=
NM_001379330.1:c.906T>C	NP_001366259.1:p.Gly302=
NM_001379331.1:c.903T>C	NP_001366260.1:p.Gly301=
NM_001379332.1:c.1053T>C	NP_001366261.1:p.Gly351=
NM_001379333.1:c.1050T>C	NP_001366262.1:p.Gly350=
NM_001379334.1:c.981T>C	NP_001366263.1:p.Gly327=