Canonical Allele Identifier: CA410376022
Gene: TMPRSS3 HGNC NCBI

Linked Data

dbSNP Id: rs1421236349

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.42390028G>A , CM000683.2:g.42390028G>A GRCh38
NC_000021.8:g.43810137G>A , CM000683.1:g.43810137G>A GRCh37
NC_000021.7:g.42683206G>A NCBI36
NG_011629.1:g.11064C>T
NG_011629.2:g.11064C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000433957.7:c.104C>T ENSP00000411013.3:p.Ala35Val
ENST00000644384.2:c.104C>T MANE Select ENSP00000494414.1:p.Ala35Val
ENST00000652415.1:c.104C>T ENSP00000498756.1:p.Ala35Val
ENST00000291532.7:c.104C>T ENSP00000291532.3:p.Ala35Val
ENST00000398397.3:c.104C>T ENSP00000381434.3:p.Ala35Val
ENST00000398405.5:c.98C>T ENSP00000381442.1:p.Ala33Val
ENST00000433957.6:c.104C>T ENSP00000411013.2:p.Ala35Val
ENST00000482761.1:n.391C>T
NM_001256317.1:c.104C>T NP_001243246.1:p.Ala35Val
NM_024022.2:c.104C>T NP_076927.1:p.Ala35Val
NM_032405.1:c.104C>T NP_115781.1:p.Ala35Val
NR_046020.1:n.1060C>T
NM_001256317.2:c.104C>T NP_001243246.1:p.Ala35Val
NM_024022.3:c.104C>T NP_076927.1:p.Ala35Val
NM_032405.2:c.104C>T NP_115781.1:p.Ala35Val
NM_001256317.3:c.104C>T MANE Select NP_001243246.1:p.Ala35Val
NM_024022.4:c.104C>T NP_076927.1:p.Ala35Val