Canonical Allele Identifier: CA193993481
Community Standard Title: NC_000009.12:g.69173834G>A
Gene: TJP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.69173834G>A , CM000671.2:g.69173834G>A GRCh38
NC_000009.11:g.71788750G>A , CM000671.1:g.71788750G>A GRCh37
NC_000009.10:g.70978570G>A NCBI36
NG_016342.1:g.57527G>A
NG_016342.2:g.77928G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001170414.2:c.-10+22063G>A NP_001163885.1:n.-10+22063G>A
NM_001369870.1:c.-10+22063G>A NP_001356799.1:n.-10+22063G>A
NM_001369871.1:c.-127-11253G>A NP_001356800.1:n.-127-11253G>A
ENST00000377259.5:c.-10+22063G>A ENSP00000366469.1:n.-10+22063G>A
ENST00000423935.5:c.-10+22063G>A ENSP00000402941.1:n.-10+22063G>A
ENST00000423935.6:c.-10+22063G>A ENSP00000402941.1:n.-10+22063G>A
ENST00000453658.6:c.-10+22063G>A ENSP00000392178.2:n.-10+22063G>A
ENST00000606364.5:c.-10+22063G>A ENSP00000475926.1:n.-10+22063G>A
ENST00000636438.1:c.237+22063G>A ENSP00000489860.1:n.237+22063G>A
ENST00000642889.1:c.447+22063G>A ENSP00000493780.1:n.447+22063G>A
ENST00000643352.1:c.*248+22063G>A ENSP00000496488.1:n.*248+22063G>A
ENST00000643713.1:c.-10+22063G>A ENSP00000494704.1:n.-10+22063G>A
ENST00000643765.1:c.762+22063G>A
ENST00000645088.1:c.*367+22063G>A ENSP00000495447.1:n.*367+22063G>A
ENST00000646862.1:c.666+22063G>A ENSP00000494599.1:n.666+22063G>A
ENST00000647986.1:c.-127-11253G>A ENSP00000496877.1:n.-127-11253G>A
ENST00000648087.1:n.377+22063G>A
XM_011519204.1:c.-10+22063G>A XP_011517506.1:n.-10+22063G>A
XM_011519205.1:c.-10+22063G>A XP_011517507.1:n.-10+22063G>A
XM_011519206.1:c.-10+22063G>A XP_011517508.1:n.-10+22063G>A
XM_011519206.2:c.-10+22063G>A XP_011517508.1:n.-10+22063G>A
XM_011519207.1:c.-10+22063G>A XP_011517509.1:n.-10+22063G>A
XM_011519207.2:c.-10+22063G>A XP_011517509.1:n.-10+22063G>A
XM_011519208.1:c.-10+22063G>A XP_011517510.1:n.-10+22063G>A
XM_011519208.2:c.-10+22063G>A XP_011517510.1:n.-10+22063G>A