Canonical Allele Identifier: CA866306622

Gene: TJP2

Linked Data

• dbSNP Id: rs1418266128
• MyVariant Identifiers: chr9:g.71865850C>T (hg19) ; chr9:g.69250934C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.69250934C>T , CM000671.2:g.69250934C>T	GRCh38
NC_000009.11:g.71865850C>T , CM000671.1:g.71865850C>T	GRCh37
NC_000009.10:g.71055670C>T	NCBI36
NG_016342.1:g.134627C>T
NG_016342.2:g.155028C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000348208.9:c.2881-1881C>T	ENSP00000345893.4:n.2881-1881C>T
ENST00000377245.9:c.2992-101C>T MANE Select	ENSP00000366453.4:n.2992-101C>T
ENST00000498204.2:n.2318-1881C>T
ENST00000535702.6:c.2893-101C>T	ENSP00000442090.1:n.2893-101C>T
ENST00000539225.2:c.3085-101C>T	ENSP00000438262.1:n.3085-101C>T
ENST00000636438.1:c.3169-101C>T	ENSP00000489860.1:n.3169-101C>T
ENST00000642889.1:c.3379-101C>T	ENSP00000493780.1:n.3379-101C>T
ENST00000645088.1:c.*3188-101C>T	ENSP00000495447.1:n.*3188-101C>T
ENST00000648042.1:c.1377-101C>T
ENST00000649114.1:c.2881-1881C>T	ENSP00000497328.1:n.2881-1881C>T
ENST00000649134.1:c.2893-1881C>T	ENSP00000498068.1:n.2893-1881C>T
ENST00000649783.1:n.2905-101C>T
ENST00000649927.1:n.537-101C>T
ENST00000649943.1:c.2881-101C>T	ENSP00000497539.1:n.2881-101C>T
ENST00000650084.1:c.2995-101C>T	ENSP00000497861.1:n.2995-101C>T
ENST00000650333.1:c.2923-101C>T	ENSP00000496791.1:n.2923-101C>T
ENST00000650353.1:n.587-101C>T
ENST00000650460.1:c.1840-1881C>T
ENST00000650522.1:n.2404-101C>T
ENST00000348208.8:c.2881-1881C>T	ENSP00000345893.4:n.2881-1881C>T
ENST00000377245.8:c.2992-101C>T	ENSP00000366453.4:n.2992-101C>T
ENST00000453658.6:c.2812-1881C>T	ENSP00000392178.2:n.2812-1881C>T
ENST00000535702.5:c.2893-101C>T	ENSP00000442090.1:n.2893-101C>T
ENST00000539225.1:c.3085-101C>T	ENSP00000438262.1:n.3085-101C>T
NM_001170414.2:c.2812-1881C>T	NP_001163885.1:n.2812-1881C>T
NM_001170415.1:c.2893-101C>T	NP_001163886.1:n.2893-101C>T
NM_001170416.1:c.3085-101C>T	NP_001163887.1:n.3085-101C>T
NM_004817.3:c.2992-101C>T	NP_004808.2:n.2992-101C>T
NM_201629.3:c.2881-1881C>T	NP_963923.1:n.2881-1881C>T
XM_005252314.1:c.3004-101C>T	XP_005252371.1:n.3004-101C>T
XM_006717324.2:c.2986-101C>T	XP_006717387.1:n.2986-101C>T
XM_011519204.1:c.2812-101C>T	XP_011517506.1:n.2812-101C>T
XM_011519205.1:c.2923-101C>T	XP_011517507.1:n.2923-101C>T
XM_011519206.1:c.2923-101C>T	XP_011517508.1:n.2923-101C>T
XM_011519207.1:c.2923-101C>T	XP_011517509.1:n.2923-101C>T
XM_011519208.1:c.2923-101C>T	XP_011517510.1:n.2923-101C>T
XM_011519209.1:c.2923-101C>T	XP_011517511.1:n.2923-101C>T
NM_004817.4:c.2992-101C>T MANE Select	NP_004808.2:n.2992-101C>T
XM_005252314.2:c.3004-101C>T	XP_005252371.1:n.3004-101C>T
XM_011519206.2:c.2923-101C>T	XP_011517508.1:n.2923-101C>T
XM_011519207.2:c.2923-101C>T	XP_011517509.1:n.2923-101C>T
XM_011519208.2:c.2923-101C>T	XP_011517510.1:n.2923-101C>T
XM_011519209.2:c.2923-101C>T	XP_011517511.1:n.2923-101C>T
XM_017015327.2:c.2881-101C>T	XP_016870816.1:n.2881-101C>T
XM_017015328.1:c.2893-1881C>T	XP_016870817.1:n.2893-1881C>T
NM_001170416.2:c.3085-101C>T	NP_001163887.1:n.3085-101C>T
NM_001369870.1:c.2917-101C>T	NP_001356799.1:n.2917-101C>T
NM_001369871.1:c.2923-101C>T	NP_001356800.1:n.2923-101C>T
NM_001369872.1:c.2881-101C>T	NP_001356801.1:n.2881-101C>T
NM_001369873.1:c.2668-101C>T	NP_001356802.1:n.2668-101C>T
NM_001369874.1:c.2893-1881C>T	NP_001356803.1:n.2893-1881C>T
NM_001369875.1:c.3004-101C>T	NP_001356804.1:n.3004-101C>T