Canonical Allele Identifier: CA2390778219
Gene: TMPRSS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.42382059A= , CM000683.2:g.42382059A= GRCh38
NC_000021.8:g.43802168A= , CM000683.1:g.43802168A= GRCh37
NC_000021.7:g.42675237A= NCBI36
NG_011629.1:g.19033T=
NG_011629.2:g.19033T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000433957.7:c.952+6T= ENSP00000411013.3:n.952+6T=
ENST00000644384.2:c.952+6T= MANE Select ENSP00000494414.1:n.952+6T=
ENST00000652415.1:c.952+6T= ENSP00000498756.1:n.952+6T=
ENST00000291532.7:c.952+6T= ENSP00000291532.3:n.952+6T=
ENST00000398397.3:c.958T= ENSP00000381434.3:p.Ser320=
ENST00000398405.5:c.946+6T= ENSP00000381442.1:n.946+6T=
ENST00000433957.6:c.952+6T= ENSP00000411013.2:n.952+6T=
ENST00000474596.5:n.820+6T=
ENST00000476848.5:n.1687+6T=
ENST00000478680.1:n.235T=
ENST00000482761.1:n.1239+6T=
NM_001256317.1:c.952+6T= NP_001243246.1:n.952+6T=
NM_024022.2:c.952+6T= NP_076927.1:n.952+6T=
NM_032404.2:c.571+6T= NP_115780.1:n.571+6T=
NM_032405.1:c.958T= NP_115781.1:p.Ser320=
NR_046020.1:n.1908+6T=
NM_001256317.2:c.952+6T= NP_001243246.1:n.952+6T=
NM_024022.3:c.952+6T= NP_076927.1:n.952+6T=
NM_032405.2:c.958T= NP_115781.1:p.Ser320=
NM_001256317.3:c.952+6T= MANE Select NP_001243246.1:n.952+6T=
NM_024022.4:c.952+6T= NP_076927.1:n.952+6T=
NM_032404.3:c.571+6T= NP_115780.1:n.571+6T=