Canonical Allele Identifier: CA373530289

Gene: TJP2

Linked Data

• MyVariant Identifiers: chr9:g.71840283C>G (hg19) ; chr9:g.69225367C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.69225367C>G , CM000671.2:g.69225367C>G	GRCh38
NC_000009.11:g.71840283C>G , CM000671.1:g.71840283C>G	GRCh37
NC_000009.10:g.71030103C>G	NCBI36
NG_016342.1:g.109060C>G
NG_016342.2:g.129461C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348208.9:c.1016C>G	ENSP00000345893.4:p.Thr339Ser
ENST00000377245.9:c.1016C>G MANE Select	ENSP00000366453.4:p.Thr339Ser
ENST00000535702.6:c.1028C>G	ENSP00000442090.1:p.Thr343Ser
ENST00000539225.2:c.1109C>G	ENSP00000438262.1:p.Thr370Ser
ENST00000636247.1:n.1095C>G
ENST00000636438.1:c.1193C>G	ENSP00000489860.1:p.Thr398Ser
ENST00000642889.1:c.1403C>G	ENSP00000493780.1:p.Thr468Ser
ENST00000643352.1:c.*1204C>G	ENSP00000496488.1:n.*1204C>G
ENST00000645088.1:c.*1323C>G	ENSP00000495447.1:n.*1323C>G
ENST00000647986.1:c.947C>G	ENSP00000496877.1:p.Thr316Ser
ENST00000648087.1:n.1333C>G
ENST00000648153.1:n.159C>G
ENST00000648862.1:n.228C>G
ENST00000649114.1:c.1016C>G	ENSP00000497328.1:p.Thr339Ser
ENST00000649134.1:c.1028C>G	ENSP00000498068.1:p.Thr343Ser
ENST00000649783.1:n.1040C>G
ENST00000649943.1:c.1016C>G	ENSP00000497539.1:p.Thr339Ser
ENST00000650084.1:c.1019C>G	ENSP00000497861.1:p.Thr340Ser
ENST00000650333.1:c.947C>G	ENSP00000496791.1:p.Thr316Ser
ENST00000650460.1:c.289C>G
ENST00000650522.1:n.977-3817C>G
ENST00000265384.11:c.1016C>G	ENSP00000265384.7:p.Thr339Ser
ENST00000348208.8:c.1016C>G	ENSP00000345893.4:p.Thr339Ser
ENST00000377245.8:c.1016C>G	ENSP00000366453.4:p.Thr339Ser
ENST00000453658.6:c.947C>G	ENSP00000392178.2:p.Thr316Ser
ENST00000535702.5:c.1028C>G	ENSP00000442090.1:p.Thr343Ser
ENST00000539225.1:c.1109C>G	ENSP00000438262.1:p.Thr370Ser
NM_001170414.2:c.947C>G	NP_001163885.1:p.Thr316Ser
NM_001170415.1:c.1028C>G	NP_001163886.1:p.Thr343Ser
NM_001170416.1:c.1109C>G	NP_001163887.1:p.Thr370Ser
NM_001170630.1:c.1016C>G	NP_001164101.1:p.Thr339Ser
NM_004817.3:c.1016C>G	NP_004808.2:p.Thr339Ser
NM_201629.3:c.1016C>G	NP_963923.1:p.Thr339Ser
XM_005252314.1:c.1028C>G	XP_005252371.1:p.Thr343Ser
XM_006717324.2:c.1010C>G	XP_006717387.1:p.Thr337Ser
XM_011519204.1:c.947C>G	XP_011517506.1:p.Thr316Ser
XM_011519205.1:c.947C>G	XP_011517507.1:p.Thr316Ser
XM_011519206.1:c.947C>G	XP_011517508.1:p.Thr316Ser
XM_011519207.1:c.947C>G	XP_011517509.1:p.Thr316Ser
XM_011519208.1:c.947C>G	XP_011517510.1:p.Thr316Ser
XM_011519209.1:c.947C>G	XP_011517511.1:p.Thr316Ser
NM_004817.4:c.1016C>G MANE Select	NP_004808.2:p.Thr339Ser
XM_005252314.2:c.1028C>G	XP_005252371.1:p.Thr343Ser
XM_011519206.2:c.947C>G	XP_011517508.1:p.Thr316Ser
XM_011519207.2:c.947C>G	XP_011517509.1:p.Thr316Ser
XM_011519208.2:c.947C>G	XP_011517510.1:p.Thr316Ser
XM_011519209.2:c.947C>G	XP_011517511.1:p.Thr316Ser
XM_017015327.2:c.1016C>G	XP_016870816.1:p.Thr339Ser
XM_017015328.1:c.1028C>G	XP_016870817.1:p.Thr343Ser
NM_001170416.2:c.1109C>G	NP_001163887.1:p.Thr370Ser
NM_001369870.1:c.947C>G	NP_001356799.1:p.Thr316Ser
NM_001369871.1:c.947C>G	NP_001356800.1:p.Thr316Ser
NM_001369872.1:c.1016C>G	NP_001356801.1:p.Thr339Ser
NM_001369873.1:c.1016C>G	NP_001356802.1:p.Thr339Ser
NM_001369874.1:c.1028C>G	NP_001356803.1:p.Thr343Ser
NM_001369875.1:c.1028C>G	NP_001356804.1:p.Thr343Ser