Canonical Allele Identifier: CA2390779866
Gene: TMPRSS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.42385405C= , CM000683.2:g.42385405C= GRCh38
NC_000021.8:g.43805514C= , CM000683.1:g.43805514C= GRCh37
NC_000021.7:g.42678583C= NCBI36
NG_011629.1:g.15687G=
NG_011629.2:g.15687G=

Transcript Alleles

HGVS Amino-acid change
ENST00000433957.7:c.572+4G= ENSP00000411013.3:n.572+4G=
ENST00000644384.2:c.572+4G= MANE Select ENSP00000494414.1:n.572+4G=
ENST00000652415.1:c.572+4G= ENSP00000498756.1:n.572+4G=
ENST00000291532.7:c.572+4G= ENSP00000291532.3:n.572+4G=
ENST00000398397.3:c.572+4G= ENSP00000381434.3:n.572+4G=
ENST00000398405.5:c.566+4G= ENSP00000381442.1:n.566+4G=
ENST00000433957.6:c.572+4G= ENSP00000411013.2:n.572+4G=
ENST00000474596.5:n.440+4G=
ENST00000482761.1:n.859+4G=
NM_001256317.1:c.572+4G= NP_001243246.1:n.572+4G=
NM_024022.2:c.572+4G= NP_076927.1:n.572+4G=
NM_032404.2:c.191+4G= NP_115780.1:n.191+4G=
NM_032405.1:c.572+4G= NP_115781.1:n.572+4G=
NR_046020.1:n.1528+4G=
NM_001256317.2:c.572+4G= NP_001243246.1:n.572+4G=
NM_024022.3:c.572+4G= NP_076927.1:n.572+4G=
NM_032405.2:c.572+4G= NP_115781.1:n.572+4G=
NM_001256317.3:c.572+4G= MANE Select NP_001243246.1:n.572+4G=
NM_024022.4:c.572+4G= NP_076927.1:n.572+4G=
NM_032404.3:c.191+4G= NP_115780.1:n.191+4G=