Canonical Allele Identifier: CA5073038

Gene: TJP2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.69221134_69221145del , CM000671.2:g.69221134_69221145del	GRCh38
NC_000009.11:g.71836050_71836061del , CM000671.1:g.71836050_71836061del	GRCh37
NC_000009.10:g.71025870_71025881del	NCBI36
NG_016342.1:g.104827_104838del
NG_016342.2:g.125228_125239del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348208.9:c.590_601del	ENSP00000345893.4:p.Arg197_Ser200del
ENST00000377245.9:c.590_601del MANE Select	ENSP00000366453.4:p.Arg197_Ser200del
ENST00000535702.6:c.602_613del	ENSP00000442090.1:p.Arg201_Ser204del
ENST00000539225.2:c.683_694del	ENSP00000438262.1:p.Arg228_Ser231del
ENST00000636247.1:n.669_680del
ENST00000636438.1:c.767_778del	ENSP00000489860.1:p.Arg256_Ser259del
ENST00000642889.1:c.977_988del	ENSP00000493780.1:p.Arg326_Ser329del
ENST00000643352.1:c.*778_*789del	ENSP00000496488.1:n.*778_*789del
ENST00000645088.1:c.*897_*908del	ENSP00000495447.1:n.*897_*908del
ENST00000647986.1:c.521_532del	ENSP00000496877.1:p.Arg174_Ser177del
ENST00000648087.1:n.907_918del
ENST00000649114.1:c.590_601del	ENSP00000497328.1:p.Arg197_Ser200del
ENST00000649134.1:c.602_613del	ENSP00000498068.1:p.Arg201_Ser204del
ENST00000649783.1:n.614_625del
ENST00000649943.1:c.590_601del	ENSP00000497539.1:p.Arg197_Ser200del
ENST00000650084.1:c.593_604del	ENSP00000497861.1:p.Arg198_Ser201del
ENST00000650333.1:c.521_532del	ENSP00000496791.1:p.Arg174_Ser177del
ENST00000650378.1:n.618_629del
ENST00000650522.1:n.614_625del
ENST00000265384.11:c.590_601del	ENSP00000265384.7:p.Arg197_Ser200del
ENST00000348208.8:c.590_601del	ENSP00000345893.4:p.Arg197_Ser200del
ENST00000377245.8:c.590_601del	ENSP00000366453.4:p.Arg197_Ser200del
ENST00000453658.6:c.521_532del	ENSP00000392178.2:p.Arg174_Ser177del
ENST00000535702.5:c.602_613del	ENSP00000442090.1:p.Arg201_Ser204del
ENST00000539225.1:c.683_694del	ENSP00000438262.1:p.Arg228_Ser231del
NM_001170414.2:c.521_532del	NP_001163885.1:p.Arg174_Ser177del
NM_001170415.1:c.602_613del	NP_001163886.1:p.Arg201_Ser204del
NM_001170416.1:c.683_694del	NP_001163887.1:p.Arg228_Ser231del
NM_001170630.1:c.590_601del	NP_001164101.1:p.Arg197_Ser200del
NM_004817.3:c.590_601del	NP_004808.2:p.Arg197_Ser200del
NM_201629.3:c.590_601del	NP_963923.1:p.Arg197_Ser200del
XM_005252314.1:c.602_613del	XP_005252371.1:p.Arg201_Ser204del
XM_006717324.2:c.584_595del	XP_006717387.1:p.Arg195_Ser198del
XM_011519204.1:c.521_532del	XP_011517506.1:p.Arg174_Ser177del
XM_011519205.1:c.521_532del	XP_011517507.1:p.Arg174_Ser177del
XM_011519206.1:c.521_532del	XP_011517508.1:p.Arg174_Ser177del
XM_011519207.1:c.521_532del	XP_011517509.1:p.Arg174_Ser177del
XM_011519208.1:c.521_532del	XP_011517510.1:p.Arg174_Ser177del
XM_011519209.1:c.521_532del	XP_011517511.1:p.Arg174_Ser177del
NM_004817.4:c.590_601del MANE Select	NP_004808.2:p.Arg197_Ser200del
XM_005252314.2:c.602_613del	XP_005252371.1:p.Arg201_Ser204del
XM_011519206.2:c.521_532del	XP_011517508.1:p.Arg174_Ser177del
XM_011519207.2:c.521_532del	XP_011517509.1:p.Arg174_Ser177del
XM_011519208.2:c.521_532del	XP_011517510.1:p.Arg174_Ser177del
XM_011519209.2:c.521_532del	XP_011517511.1:p.Arg174_Ser177del
XM_017015327.2:c.590_601del	XP_016870816.1:p.Arg197_Ser200del
XM_017015328.1:c.602_613del	XP_016870817.1:p.Arg201_Ser204del
NM_001170416.2:c.683_694del	NP_001163887.1:p.Arg228_Ser231del
NM_001369870.1:c.521_532del	NP_001356799.1:p.Arg174_Ser177del
NM_001369871.1:c.521_532del	NP_001356800.1:p.Arg174_Ser177del
NM_001369872.1:c.590_601del	NP_001356801.1:p.Arg197_Ser200del
NM_001369873.1:c.590_601del	NP_001356802.1:p.Arg197_Ser200del
NM_001369874.1:c.602_613del	NP_001356803.1:p.Arg201_Ser204del
NM_001369875.1:c.602_613del	NP_001356804.1:p.Arg201_Ser204del