Canonical Allele Identifier: CA410374754
Gene: TMPRSS3 HGNC NCBI

Linked Data

dbSNP Id: rs747054153

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.42385414A>T , CM000683.2:g.42385414A>T GRCh38
NC_000021.8:g.43805523A>T , CM000683.1:g.43805523A>T GRCh37
NC_000021.7:g.42678592A>T NCBI36
NG_011629.1:g.15678T>A
NG_011629.2:g.15678T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000433957.7:c.567T>A ENSP00000411013.3:p.Tyr189Ter
ENST00000644384.2:c.567T>A MANE Select ENSP00000494414.1:p.Tyr189Ter
ENST00000652415.1:c.567T>A ENSP00000498756.1:p.Tyr189Ter
ENST00000291532.7:c.567T>A ENSP00000291532.3:p.Tyr189Ter
ENST00000398397.3:c.567T>A ENSP00000381434.3:p.Tyr189Ter
ENST00000398405.5:c.561T>A ENSP00000381442.1:p.Tyr187Ter
ENST00000433957.6:c.567T>A ENSP00000411013.2:p.Tyr189Ter
ENST00000474596.5:n.435T>A
ENST00000482761.1:n.854T>A
NM_001256317.1:c.567T>A NP_001243246.1:p.Tyr189Ter
NM_024022.2:c.567T>A NP_076927.1:p.Tyr189Ter
NM_032404.2:c.186T>A NP_115780.1:p.Tyr62Ter
NM_032405.1:c.567T>A NP_115781.1:p.Tyr189Ter
NR_046020.1:n.1523T>A
NM_001256317.2:c.567T>A NP_001243246.1:p.Tyr189Ter
NM_024022.3:c.567T>A NP_076927.1:p.Tyr189Ter
NM_032405.2:c.567T>A NP_115781.1:p.Tyr189Ter
NM_001256317.3:c.567T>A MANE Select NP_001243246.1:p.Tyr189Ter
NM_024022.4:c.567T>A NP_076927.1:p.Tyr189Ter
NM_032404.3:c.186T>A NP_115780.1:p.Tyr62Ter