Canonical Allele Identifier: CA373536614

Gene: TJP2

Linked Data

• MyVariant Identifiers: chr9:g.71861683G>T (hg19) ; chr9:g.69246767G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.69246767G>T , CM000671.2:g.69246767G>T	GRCh38
NC_000009.11:g.71861683G>T , CM000671.1:g.71861683G>T	GRCh37
NC_000009.10:g.71051503G>T	NCBI36
NG_016342.1:g.130460G>T
NG_016342.2:g.150861G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000348208.9:c.2644G>T	ENSP00000345893.4:p.Ala882Ser
ENST00000377245.9:c.2644G>T MANE Select	ENSP00000366453.4:p.Ala882Ser
ENST00000498204.2:n.2081G>T
ENST00000535702.6:c.2656G>T	ENSP00000442090.1:p.Ala886Ser
ENST00000539225.2:c.2737G>T	ENSP00000438262.1:p.Ala913Ser
ENST00000636247.1:n.2723G>T
ENST00000636438.1:c.2821G>T	ENSP00000489860.1:p.Ala941Ser
ENST00000642889.1:c.3031G>T	ENSP00000493780.1:p.Ala1011Ser
ENST00000643352.1:c.*2832G>T	ENSP00000496488.1:n.*2832G>T
ENST00000645088.1:c.*2951G>T	ENSP00000495447.1:n.*2951G>T
ENST00000648042.1:c.1353G>T
ENST00000648087.1:n.2954G>T
ENST00000649114.1:c.2644G>T	ENSP00000497328.1:p.Ala882Ser
ENST00000649134.1:c.2656G>T	ENSP00000498068.1:p.Ala886Ser
ENST00000649783.1:n.2668G>T
ENST00000649927.1:n.189G>T
ENST00000649943.1:c.2644G>T	ENSP00000497539.1:p.Ala882Ser
ENST00000650084.1:c.2647G>T	ENSP00000497861.1:p.Ala883Ser
ENST00000650333.1:c.2575G>T	ENSP00000496791.1:p.Ala859Ser
ENST00000650460.1:c.1840-6048G>T
ENST00000650522.1:n.2167G>T
ENST00000265384.11:c.2644G>T	ENSP00000265384.7:p.Ala882Ser
ENST00000348208.8:c.2644G>T	ENSP00000345893.4:p.Ala882Ser
ENST00000377245.8:c.2644G>T	ENSP00000366453.4:p.Ala882Ser
ENST00000453658.6:c.2575G>T	ENSP00000392178.2:p.Ala859Ser
ENST00000498204.1:n.542G>T
ENST00000535702.5:c.2656G>T	ENSP00000442090.1:p.Ala886Ser
ENST00000539225.1:c.2737G>T	ENSP00000438262.1:p.Ala913Ser
NM_001170414.2:c.2575G>T	NP_001163885.1:p.Ala859Ser
NM_001170415.1:c.2656G>T	NP_001163886.1:p.Ala886Ser
NM_001170416.1:c.2737G>T	NP_001163887.1:p.Ala913Ser
NM_001170630.1:c.2644G>T	NP_001164101.1:p.Ala882Ser
NM_004817.3:c.2644G>T	NP_004808.2:p.Ala882Ser
NM_201629.3:c.2644G>T	NP_963923.1:p.Ala882Ser
XM_005252314.1:c.2656G>T	XP_005252371.1:p.Ala886Ser
XM_006717324.2:c.2638G>T	XP_006717387.1:p.Ala880Ser
XM_011519204.1:c.2575G>T	XP_011517506.1:p.Ala859Ser
XM_011519205.1:c.2575G>T	XP_011517507.1:p.Ala859Ser
XM_011519206.1:c.2575G>T	XP_011517508.1:p.Ala859Ser
XM_011519207.1:c.2575G>T	XP_011517509.1:p.Ala859Ser
XM_011519208.1:c.2575G>T	XP_011517510.1:p.Ala859Ser
XM_011519209.1:c.2575G>T	XP_011517511.1:p.Ala859Ser
NM_004817.4:c.2644G>T MANE Select	NP_004808.2:p.Ala882Ser
XM_005252314.2:c.2656G>T	XP_005252371.1:p.Ala886Ser
XM_011519206.2:c.2575G>T	XP_011517508.1:p.Ala859Ser
XM_011519207.2:c.2575G>T	XP_011517509.1:p.Ala859Ser
XM_011519208.2:c.2575G>T	XP_011517510.1:p.Ala859Ser
XM_011519209.2:c.2575G>T	XP_011517511.1:p.Ala859Ser
XM_017015327.2:c.2644G>T	XP_016870816.1:p.Ala882Ser
XM_017015328.1:c.2656G>T	XP_016870817.1:p.Ala886Ser
NM_001170416.2:c.2737G>T	NP_001163887.1:p.Ala913Ser
NM_001369870.1:c.2569G>T	NP_001356799.1:p.Ala857Ser
NM_001369871.1:c.2575G>T	NP_001356800.1:p.Ala859Ser
NM_001369872.1:c.2644G>T	NP_001356801.1:p.Ala882Ser
NM_001369873.1:c.2644G>T	NP_001356802.1:p.Ala882Ser
NM_001369874.1:c.2656G>T	NP_001356803.1:p.Ala886Ser
NM_001369875.1:c.2656G>T	NP_001356804.1:p.Ala886Ser