Canonical Allele Identifier: CA5073119

Gene: TJP2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.69221421C>T , CM000671.2:g.69221421C>T	GRCh38
NC_000009.11:g.71836337C>T , CM000671.1:g.71836337C>T	GRCh37
NC_000009.10:g.71026157C>T	NCBI36
NG_016342.1:g.105114C>T
NG_016342.2:g.125515C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348208.9:c.877C>T	ENSP00000345893.4:p.Arg293Trp
ENST00000377245.9:c.877C>T MANE Select	ENSP00000366453.4:p.Arg293Trp
ENST00000535702.6:c.889C>T	ENSP00000442090.1:p.Arg297Trp
ENST00000539225.2:c.970C>T	ENSP00000438262.1:p.Arg324Trp
ENST00000636247.1:n.956C>T
ENST00000636438.1:c.1054C>T	ENSP00000489860.1:p.Arg352Trp
ENST00000642889.1:c.1264C>T	ENSP00000493780.1:p.Arg422Trp
ENST00000643352.1:c.*1065C>T	ENSP00000496488.1:n.*1065C>T
ENST00000645088.1:c.*1184C>T	ENSP00000495447.1:n.*1184C>T
ENST00000647986.1:c.808C>T	ENSP00000496877.1:p.Arg270Trp
ENST00000648087.1:n.1194C>T
ENST00000648862.1:n.89C>T
ENST00000649114.1:c.877C>T	ENSP00000497328.1:p.Arg293Trp
ENST00000649134.1:c.889C>T	ENSP00000498068.1:p.Arg297Trp
ENST00000649783.1:n.901C>T
ENST00000649943.1:c.877C>T	ENSP00000497539.1:p.Arg293Trp
ENST00000650084.1:c.880C>T	ENSP00000497861.1:p.Arg294Trp
ENST00000650333.1:c.808C>T	ENSP00000496791.1:p.Arg270Trp
ENST00000650460.1:c.150C>T
ENST00000650522.1:n.901C>T
ENST00000265384.11:c.877C>T	ENSP00000265384.7:p.Arg293Trp
ENST00000348208.8:c.877C>T	ENSP00000345893.4:p.Arg293Trp
ENST00000377245.8:c.877C>T	ENSP00000366453.4:p.Arg293Trp
ENST00000453658.6:c.808C>T	ENSP00000392178.2:p.Arg270Trp
ENST00000535702.5:c.889C>T	ENSP00000442090.1:p.Arg297Trp
ENST00000539225.1:c.970C>T	ENSP00000438262.1:p.Arg324Trp
NM_001170414.2:c.808C>T	NP_001163885.1:p.Arg270Trp
NM_001170415.1:c.889C>T	NP_001163886.1:p.Arg297Trp
NM_001170416.1:c.970C>T	NP_001163887.1:p.Arg324Trp
NM_001170630.1:c.877C>T	NP_001164101.1:p.Arg293Trp
NM_004817.3:c.877C>T	NP_004808.2:p.Arg293Trp
NM_201629.3:c.877C>T	NP_963923.1:p.Arg293Trp
XM_005252314.1:c.889C>T	XP_005252371.1:p.Arg297Trp
XM_006717324.2:c.871C>T	XP_006717387.1:p.Arg291Trp
XM_011519204.1:c.808C>T	XP_011517506.1:p.Arg270Trp
XM_011519205.1:c.808C>T	XP_011517507.1:p.Arg270Trp
XM_011519206.1:c.808C>T	XP_011517508.1:p.Arg270Trp
XM_011519207.1:c.808C>T	XP_011517509.1:p.Arg270Trp
XM_011519208.1:c.808C>T	XP_011517510.1:p.Arg270Trp
XM_011519209.1:c.808C>T	XP_011517511.1:p.Arg270Trp
NM_004817.4:c.877C>T MANE Select	NP_004808.2:p.Arg293Trp
XM_005252314.2:c.889C>T	XP_005252371.1:p.Arg297Trp
XM_011519206.2:c.808C>T	XP_011517508.1:p.Arg270Trp
XM_011519207.2:c.808C>T	XP_011517509.1:p.Arg270Trp
XM_011519208.2:c.808C>T	XP_011517510.1:p.Arg270Trp
XM_011519209.2:c.808C>T	XP_011517511.1:p.Arg270Trp
XM_017015327.2:c.877C>T	XP_016870816.1:p.Arg293Trp
XM_017015328.1:c.889C>T	XP_016870817.1:p.Arg297Trp
NM_001170416.2:c.970C>T	NP_001163887.1:p.Arg324Trp
NM_001369870.1:c.808C>T	NP_001356799.1:p.Arg270Trp
NM_001369871.1:c.808C>T	NP_001356800.1:p.Arg270Trp
NM_001369872.1:c.877C>T	NP_001356801.1:p.Arg293Trp
NM_001369873.1:c.877C>T	NP_001356802.1:p.Arg293Trp
NM_001369874.1:c.889C>T	NP_001356803.1:p.Arg297Trp
NM_001369875.1:c.889C>T	NP_001356804.1:p.Arg297Trp