Canonical Allele Identifier: CA588209128

Gene: TJP2

Linked Data

• dbSNP Id: rs1269580450
• gnomAD v2: 9-71831241-TC-T
• gnomAD v3: 9-69216325-TC-T
• gnomAD v4: 9-69216325-TC-T
• MyVariant Identifiers: chr9:g.71831242del (hg19) ; chr9:g.69216326del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.69216326del , CM000671.2:g.69216326del	GRCh38
NC_000009.11:g.71831242del , CM000671.1:g.71831242del	GRCh37
NC_000009.10:g.71021062del	NCBI36
NG_016342.1:g.100019del
NG_016342.2:g.120420del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348208.9:c.115-13del	ENSP00000345893.4:n.115-13del
ENST00000377245.9:c.115-13del MANE Select	ENSP00000366453.4:n.115-13del
ENST00000423935.6:c.46-13del	ENSP00000402941.1:n.46-13del
ENST00000535702.6:c.127-13del	ENSP00000442090.1:n.127-13del
ENST00000539225.2:c.208-13del	ENSP00000438262.1:n.208-13del
ENST00000636247.1:n.194-13del
ENST00000636438.1:c.292-13del	ENSP00000489860.1:n.292-13del
ENST00000642889.1:c.502-13del	ENSP00000493780.1:n.502-13del
ENST00000643352.1:c.*303-13del	ENSP00000496488.1:n.*303-13del
ENST00000643765.1:c.817-13del
ENST00000645088.1:c.*422-13del	ENSP00000495447.1:n.*422-13del
ENST00000647986.1:c.46-13del	ENSP00000496877.1:n.46-13del
ENST00000648087.1:n.432-13del
ENST00000648402.1:c.46-13del	ENSP00000497596.1:n.46-13del
ENST00000649114.1:c.115-13del	ENSP00000497328.1:n.115-13del
ENST00000649134.1:c.127-13del	ENSP00000498068.1:n.127-13del
ENST00000649783.1:n.139-13del
ENST00000649939.1:c.46-13del	ENSP00000498043.1:n.46-13del
ENST00000649943.1:c.115-13del	ENSP00000497539.1:n.115-13del
ENST00000650084.1:c.118-13del	ENSP00000497861.1:n.118-13del
ENST00000650333.1:c.46-13del	ENSP00000496791.1:n.46-13del
ENST00000650378.1:n.143-13del
ENST00000650522.1:n.139-13del
ENST00000265384.11:c.115-13del	ENSP00000265384.7:n.115-13del
ENST00000348208.8:c.115-13del	ENSP00000345893.4:n.115-13del
ENST00000377245.8:c.115-13del	ENSP00000366453.4:n.115-13del
ENST00000377259.5:c.46-13del	ENSP00000366469.1:n.46-13del
ENST00000423935.5:c.46-13del	ENSP00000402941.1:n.46-13del
ENST00000453658.6:c.46-13del	ENSP00000392178.2:n.46-13del
ENST00000535702.5:c.127-13del	ENSP00000442090.1:n.127-13del
ENST00000539225.1:c.208-13del	ENSP00000438262.1:n.208-13del
ENST00000606364.5:c.46-13del	ENSP00000475926.1:n.46-13del
NM_001170414.2:c.46-13del	NP_001163885.1:n.46-13del
NM_001170415.1:c.127-13del	NP_001163886.1:n.127-13del
NM_001170416.1:c.208-13del	NP_001163887.1:n.208-13del
NM_001170630.1:c.115-13del	NP_001164101.1:n.115-13del
NM_004817.3:c.115-13del	NP_004808.2:n.115-13del
NM_201629.3:c.115-13del	NP_963923.1:n.115-13del
XM_005252314.1:c.127-13del	XP_005252371.1:n.127-13del
XM_006717324.2:c.109-13del	XP_006717387.1:n.109-13del
XM_011519204.1:c.46-13del	XP_011517506.1:n.46-13del
XM_011519205.1:c.46-13del	XP_011517507.1:n.46-13del
XM_011519206.1:c.46-13del	XP_011517508.1:n.46-13del
XM_011519207.1:c.46-13del	XP_011517509.1:n.46-13del
XM_011519208.1:c.46-13del	XP_011517510.1:n.46-13del
XM_011519209.1:c.46-13del	XP_011517511.1:n.46-13del
NM_004817.4:c.115-13del MANE Select	NP_004808.2:n.115-13del
XM_005252314.2:c.127-13del	XP_005252371.1:n.127-13del
XM_011519206.2:c.46-13del	XP_011517508.1:n.46-13del
XM_011519207.2:c.46-13del	XP_011517509.1:n.46-13del
XM_011519208.2:c.46-13del	XP_011517510.1:n.46-13del
XM_011519209.2:c.46-13del	XP_011517511.1:n.46-13del
XM_017015327.2:c.115-13del	XP_016870816.1:n.115-13del
XM_017015328.1:c.127-13del	XP_016870817.1:n.127-13del
NM_001170416.2:c.208-13del	NP_001163887.1:n.208-13del
NM_001369870.1:c.46-13del	NP_001356799.1:n.46-13del
NM_001369871.1:c.46-13del	NP_001356800.1:n.46-13del
NM_001369872.1:c.115-13del	NP_001356801.1:n.115-13del
NM_001369873.1:c.115-13del	NP_001356802.1:n.115-13del
NM_001369874.1:c.127-13del	NP_001356803.1:n.127-13del
NM_001369875.1:c.127-13del	NP_001356804.1:n.127-13del