Canonical Allele Identifier: CA465254207

Gene: TJP2

Linked Data

• MyVariant Identifiers: chr9:g.71861679A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.69246763A>T , CM000671.2:g.69246763A>T	GRCh38
NC_000009.11:g.71861679A>T , CM000671.1:g.71861679A>T	GRCh37
NC_000009.10:g.71051499A>T	NCBI36
NG_016342.1:g.130456A>T
NG_016342.2:g.150857A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000348208.9:c.2640A>T	ENSP00000345893.4:p.Gly880=
ENST00000377245.9:c.2640A>T MANE Select	ENSP00000366453.4:p.Gly880=
ENST00000498204.2:n.2077A>T
ENST00000535702.6:c.2652A>T	ENSP00000442090.1:p.Gly884=
ENST00000539225.2:c.2733A>T	ENSP00000438262.1:p.Gly911=
ENST00000636247.1:n.2719A>T
ENST00000636438.1:c.2817A>T	ENSP00000489860.1:p.Gly939=
ENST00000642889.1:c.3027A>T	ENSP00000493780.1:p.Gly1009=
ENST00000643352.1:c.*2828A>T	ENSP00000496488.1:n.*2828A>T
ENST00000645088.1:c.*2947A>T	ENSP00000495447.1:n.*2947A>T
ENST00000648042.1:c.1349A>T
ENST00000648087.1:n.2950A>T
ENST00000649114.1:c.2640A>T	ENSP00000497328.1:p.Gly880=
ENST00000649134.1:c.2652A>T	ENSP00000498068.1:p.Gly884=
ENST00000649783.1:n.2664A>T
ENST00000649927.1:n.185A>T
ENST00000649943.1:c.2640A>T	ENSP00000497539.1:p.Gly880=
ENST00000650084.1:c.2643A>T	ENSP00000497861.1:p.Gly881=
ENST00000650333.1:c.2571A>T	ENSP00000496791.1:p.Gly857=
ENST00000650460.1:c.1840-6052A>T
ENST00000650522.1:n.2163A>T
ENST00000265384.11:c.2640A>T	ENSP00000265384.7:p.Gly880=
ENST00000348208.8:c.2640A>T	ENSP00000345893.4:p.Gly880=
ENST00000377245.8:c.2640A>T	ENSP00000366453.4:p.Gly880=
ENST00000453658.6:c.2571A>T	ENSP00000392178.2:p.Gly857=
ENST00000498204.1:n.538A>T
ENST00000535702.5:c.2652A>T	ENSP00000442090.1:p.Gly884=
ENST00000539225.1:c.2733A>T	ENSP00000438262.1:p.Gly911=
NM_001170414.2:c.2571A>T	NP_001163885.1:p.Gly857=
NM_001170415.1:c.2652A>T	NP_001163886.1:p.Gly884=
NM_001170416.1:c.2733A>T	NP_001163887.1:p.Gly911=
NM_001170630.1:c.2640A>T	NP_001164101.1:p.Gly880=
NM_004817.3:c.2640A>T	NP_004808.2:p.Gly880=
NM_201629.3:c.2640A>T	NP_963923.1:p.Gly880=
XM_005252314.1:c.2652A>T	XP_005252371.1:p.Gly884=
XM_006717324.2:c.2634A>T	XP_006717387.1:p.Gly878=
XM_011519204.1:c.2571A>T	XP_011517506.1:p.Gly857=
XM_011519205.1:c.2571A>T	XP_011517507.1:p.Gly857=
XM_011519206.1:c.2571A>T	XP_011517508.1:p.Gly857=
XM_011519207.1:c.2571A>T	XP_011517509.1:p.Gly857=
XM_011519208.1:c.2571A>T	XP_011517510.1:p.Gly857=
XM_011519209.1:c.2571A>T	XP_011517511.1:p.Gly857=
NM_004817.4:c.2640A>T MANE Select	NP_004808.2:p.Gly880=
XM_005252314.2:c.2652A>T	XP_005252371.1:p.Gly884=
XM_011519206.2:c.2571A>T	XP_011517508.1:p.Gly857=
XM_011519207.2:c.2571A>T	XP_011517509.1:p.Gly857=
XM_011519208.2:c.2571A>T	XP_011517510.1:p.Gly857=
XM_011519209.2:c.2571A>T	XP_011517511.1:p.Gly857=
XM_017015327.2:c.2640A>T	XP_016870816.1:p.Gly880=
XM_017015328.1:c.2652A>T	XP_016870817.1:p.Gly884=
NM_001170416.2:c.2733A>T	NP_001163887.1:p.Gly911=
NM_001369870.1:c.2565A>T	NP_001356799.1:p.Gly855=
NM_001369871.1:c.2571A>T	NP_001356800.1:p.Gly857=
NM_001369872.1:c.2640A>T	NP_001356801.1:p.Gly880=
NM_001369873.1:c.2640A>T	NP_001356802.1:p.Gly880=
NM_001369874.1:c.2652A>T	NP_001356803.1:p.Gly884=
NM_001369875.1:c.2652A>T	NP_001356804.1:p.Gly884=