Canonical Allele Identifier: CA465243339

Gene: TJP2

Linked Data

• MyVariant Identifiers: chr9:g.71840281A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.69225365A>G , CM000671.2:g.69225365A>G	GRCh38
NC_000009.11:g.71840281A>G , CM000671.1:g.71840281A>G	GRCh37
NC_000009.10:g.71030101A>G	NCBI36
NG_016342.1:g.109058A>G
NG_016342.2:g.129459A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348208.9:c.1014A>G	ENSP00000345893.4:p.Ala338=
ENST00000377245.9:c.1014A>G MANE Select	ENSP00000366453.4:p.Ala338=
ENST00000535702.6:c.1026A>G	ENSP00000442090.1:p.Ala342=
ENST00000539225.2:c.1107A>G	ENSP00000438262.1:p.Ala369=
ENST00000636247.1:n.1093A>G
ENST00000636438.1:c.1191A>G	ENSP00000489860.1:p.Ala397=
ENST00000642889.1:c.1401A>G	ENSP00000493780.1:p.Ala467=
ENST00000643352.1:c.*1202A>G	ENSP00000496488.1:n.*1202A>G
ENST00000645088.1:c.*1321A>G	ENSP00000495447.1:n.*1321A>G
ENST00000647986.1:c.945A>G	ENSP00000496877.1:p.Ala315=
ENST00000648087.1:n.1331A>G
ENST00000648153.1:n.157A>G
ENST00000648862.1:n.226A>G
ENST00000649114.1:c.1014A>G	ENSP00000497328.1:p.Ala338=
ENST00000649134.1:c.1026A>G	ENSP00000498068.1:p.Ala342=
ENST00000649783.1:n.1038A>G
ENST00000649943.1:c.1014A>G	ENSP00000497539.1:p.Ala338=
ENST00000650084.1:c.1017A>G	ENSP00000497861.1:p.Ala339=
ENST00000650333.1:c.945A>G	ENSP00000496791.1:p.Ala315=
ENST00000650460.1:c.287A>G
ENST00000650522.1:n.977-3819A>G
ENST00000265384.11:c.1014A>G	ENSP00000265384.7:p.Ala338=
ENST00000348208.8:c.1014A>G	ENSP00000345893.4:p.Ala338=
ENST00000377245.8:c.1014A>G	ENSP00000366453.4:p.Ala338=
ENST00000453658.6:c.945A>G	ENSP00000392178.2:p.Ala315=
ENST00000535702.5:c.1026A>G	ENSP00000442090.1:p.Ala342=
ENST00000539225.1:c.1107A>G	ENSP00000438262.1:p.Ala369=
NM_001170414.2:c.945A>G	NP_001163885.1:p.Ala315=
NM_001170415.1:c.1026A>G	NP_001163886.1:p.Ala342=
NM_001170416.1:c.1107A>G	NP_001163887.1:p.Ala369=
NM_001170630.1:c.1014A>G	NP_001164101.1:p.Ala338=
NM_004817.3:c.1014A>G	NP_004808.2:p.Ala338=
NM_201629.3:c.1014A>G	NP_963923.1:p.Ala338=
XM_005252314.1:c.1026A>G	XP_005252371.1:p.Ala342=
XM_006717324.2:c.1008A>G	XP_006717387.1:p.Ala336=
XM_011519204.1:c.945A>G	XP_011517506.1:p.Ala315=
XM_011519205.1:c.945A>G	XP_011517507.1:p.Ala315=
XM_011519206.1:c.945A>G	XP_011517508.1:p.Ala315=
XM_011519207.1:c.945A>G	XP_011517509.1:p.Ala315=
XM_011519208.1:c.945A>G	XP_011517510.1:p.Ala315=
XM_011519209.1:c.945A>G	XP_011517511.1:p.Ala315=
NM_004817.4:c.1014A>G MANE Select	NP_004808.2:p.Ala338=
XM_005252314.2:c.1026A>G	XP_005252371.1:p.Ala342=
XM_011519206.2:c.945A>G	XP_011517508.1:p.Ala315=
XM_011519207.2:c.945A>G	XP_011517509.1:p.Ala315=
XM_011519208.2:c.945A>G	XP_011517510.1:p.Ala315=
XM_011519209.2:c.945A>G	XP_011517511.1:p.Ala315=
XM_017015327.2:c.1014A>G	XP_016870816.1:p.Ala338=
XM_017015328.1:c.1026A>G	XP_016870817.1:p.Ala342=
NM_001170416.2:c.1107A>G	NP_001163887.1:p.Ala369=
NM_001369870.1:c.945A>G	NP_001356799.1:p.Ala315=
NM_001369871.1:c.945A>G	NP_001356800.1:p.Ala315=
NM_001369872.1:c.1014A>G	NP_001356801.1:p.Ala338=
NM_001369873.1:c.1014A>G	NP_001356802.1:p.Ala338=
NM_001369874.1:c.1026A>G	NP_001356803.1:p.Ala342=
NM_001369875.1:c.1026A>G	NP_001356804.1:p.Ala342=