Canonical Allele Identifier: CA394728198

Gene: CIITA

Linked Data

• MyVariant Identifiers: chr16:g.10995928T>C (hg19) ; chr16:g.10902071T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10902071T>C , CM000678.2:g.10902071T>C	GRCh38
NC_000016.9:g.10995928T>C , CM000678.1:g.10995928T>C	GRCh37
NC_000016.8:g.10903429T>C	NCBI36
NG_009628.1:g.29874T>C , LRG_49:g.29874T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000695879.1:n.540T>C
ENST00000324288.14:c.515T>C MANE Select	ENSP00000316328.8:p.Leu172Pro
ENST00000637439.1:c.749T>C	ENSP00000489907.1:p.Leu250Pro
ENST00000324288.12:c.515T>C	ENSP00000316328.8:p.Leu172Pro
ENST00000381835.9:c.481+513T>C	ENSP00000371257.5:n.481+513T>C
ENST00000537380.1:n.515T>C
ENST00000570546.5:n.636T>C
ENST00000571186.5:c.*236T>C	ENSP00000459829.1:n.*236T>C
ENST00000573309.5:n.599+513T>C
ENST00000576601.1:c.443T>C	ENSP00000459608.1:p.Leu148Pro
ENST00000611587.4:c.484+513T>C	ENSP00000483487.1:n.484+513T>C
ENST00000618207.4:c.515T>C	ENSP00000484761.1:p.Leu172Pro
ENST00000618327.4:c.518T>C	ENSP00000485010.1:p.Leu173Pro
NM_000246.3:c.515T>C , LRG_49t1:c.515T>C	NP_000237.2:p.Leu172Pro
NM_001286402.1:c.518T>C	NP_001273331.1:p.Leu173Pro
NM_001286403.1:c.481+513T>C	NP_001273332.1:n.481+513T>C
NR_104444.1:n.648T>C
XM_006720880.2:c.812T>C	XP_006720943.2:p.Leu271Pro
XM_011522484.1:c.812T>C	XP_011520786.1:p.Leu271Pro
XM_011522485.1:c.812T>C	XP_011520787.1:p.Leu271Pro
XM_011522486.1:c.812T>C	XP_011520788.1:p.Leu271Pro
XM_011522487.1:c.679+513T>C	XP_011520789.1:n.679+513T>C
XM_011522488.1:c.563T>C	XP_011520790.1:p.Leu188Pro
XM_011522489.1:c.676+513T>C	XP_011520791.1:n.676+513T>C
XM_011522490.1:c.560T>C	XP_011520792.1:p.Leu187Pro
XM_011522491.1:c.812T>C	XP_011520793.1:p.Leu271Pro
XM_011522492.1:c.518T>C	XP_011520794.1:p.Leu173Pro
XM_011522493.1:c.515T>C	XP_011520795.1:p.Leu172Pro
XM_011522494.1:c.446T>C	XP_011520796.1:p.Leu149Pro
XM_011522495.1:c.484+513T>C	XP_011520797.1:n.484+513T>C
XM_011522496.1:c.481+513T>C	XP_011520798.1:n.481+513T>C
XR_932841.1:n.827T>C
XR_932842.1:n.827T>C
XR_932843.1:n.827T>C
XR_932846.1:n.827T>C
XR_932847.1:n.827T>C
XR_932848.1:n.631+513T>C
XM_006720880.3:c.812T>C	XP_006720943.2:p.Leu271Pro
XM_011522484.3:c.812T>C	XP_011520786.1:p.Leu271Pro
XM_011522485.2:c.812T>C	XP_011520787.1:p.Leu271Pro
XM_011522486.2:c.812T>C	XP_011520788.1:p.Leu271Pro
XM_011522487.2:c.679+513T>C	XP_011520789.1:n.679+513T>C
XM_011522488.2:c.563T>C	XP_011520790.1:p.Leu188Pro
XM_011522489.2:c.676+513T>C	XP_011520791.1:n.676+513T>C
XM_011522490.2:c.560T>C	XP_011520792.1:p.Leu187Pro
XM_011522491.2:c.812T>C	XP_011520793.1:p.Leu271Pro
XM_011522492.2:c.518T>C	XP_011520794.1:p.Leu173Pro
XM_011522493.2:c.515T>C	XP_011520795.1:p.Leu172Pro
XM_011522494.2:c.446T>C	XP_011520796.1:p.Leu149Pro
XM_011522495.2:c.484+513T>C	XP_011520797.1:n.484+513T>C
XM_011522496.2:c.481+513T>C	XP_011520798.1:n.481+513T>C
XM_024450280.1:c.758T>C	XP_024306048.1:p.Leu253Pro
XM_024450281.1:c.724+513T>C	XP_024306049.1:n.724+513T>C
XR_001751904.1:n.831T>C
XR_932841.3:n.829T>C
XR_932842.2:n.829T>C
XR_932846.3:n.831T>C
XR_932847.3:n.831T>C
NM_001286403.2:c.481+513T>C	NP_001273332.1:n.481+513T>C
NR_104444.2:n.644T>C
NM_000246.4:c.515T>C MANE Select	NP_000237.2:p.Leu172Pro
NM_001379330.1:c.484+513T>C	NP_001366259.1:n.484+513T>C
NM_001379331.1:c.481+513T>C	NP_001366260.1:n.481+513T>C
NM_001379332.1:c.518T>C	NP_001366261.1:p.Leu173Pro
NM_001379333.1:c.515T>C	NP_001366262.1:p.Leu172Pro
NM_001379334.1:c.446T>C	NP_001366263.1:p.Leu149Pro