Canonical Allele Identifier: CA1139829773
Gene: TSNAX HGNC NCBI
TSNAX-DISC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.231557942G= , CM000663.2:g.231557942G= GRCh38
NC_000001.10:g.231693688G= , CM000663.1:g.231693688G= GRCh37
NC_000001.9:g.229760311G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000366639.9:c.368-3186G= (TSNAX) MANE Select ENSP00000355599.3:n.368-3186G=
ENST00000413309.3:c.389-3186G= (TSNAX) ENSP00000397537.1:n.389-3186G=
ENST00000644515.1:c.367+15331G= (TSNAX-DISC1) ENSP00000496433.1:n.367+15331G=
ENST00000646525.1:c.367+15331G= (TSNAX-DISC1) ENSP00000494923.1:n.367+15331G=
ENST00000647072.1:c.367+15331G= (TSNAX-DISC1) ENSP00000493799.1:n.367+15331G=
ENST00000366639.8:c.368-3186G= (TSNAX) ENSP00000355599.3:n.368-3186G=
ENST00000413309.2:c.389-3186G= (TSNAX) ENSP00000397537.1:n.389-3186G=
ENST00000475168.1:n.3340-3186G= (TSNAX)
ENST00000602567.1:c.368-3186G= (TSNAX-DISC1) ENSP00000473456.1:n.368-3186G=
ENST00000602634.5:c.367+15331G= (TSNAX-DISC1) ENSP00000473307.1:n.367+15331G=
ENST00000602885.5:c.122-3186G= (TSNAX-DISC1) ENSP00000473476.1:n.122-3186G=
ENST00000602956.5:c.368-3186G= (TSNAX-DISC1) ENSP00000473532.1:n.368-3186G=
ENST00000602962.5:c.368-3186G= (TSNAX-DISC1) ENSP00000473367.1:n.368-3186G=
NM_005999.2:c.368-3186G= (TSNAX) NP_005990.1:n.368-3186G=
NR_028393.1:n.525+15331G= (TSNAX-DISC1)
NR_028394.1:n.526-3186G= (TSNAX-DISC1)
NR_028395.1:n.526-3186G= (TSNAX-DISC1)
NR_028396.1:n.525+15331G= (TSNAX-DISC1)
NR_028397.1:n.526-3186G= (TSNAX-DISC1)
NR_028398.1:n.280-3186G= (TSNAX-DISC1)
NR_028399.1:n.526-3186G= (TSNAX-DISC1)
NR_028400.1:n.525+15331G= (TSNAX-DISC1)
NM_005999.3:c.368-3186G= (TSNAX) MANE Select NP_005990.1:n.368-3186G=