Canonical Allele Identifier: CA137692
Gene: TMPRSS3 HGNC NCBI

Linked Data

ClinVar Variation Id: 46105
dbSNP Id: rs928302

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.42389975C>T , CM000683.2:g.42389975C>T GRCh38
NC_000021.8:g.43810084C>T , CM000683.1:g.43810084C>T GRCh37
NC_000021.7:g.42683153C>T NCBI36
NG_011629.1:g.11117G>A
NG_011629.2:g.11117G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000433957.7:c.157G>A ENSP00000411013.3:p.Val53Ile
ENST00000644384.2:c.157G>A MANE Select ENSP00000494414.1:p.Val53Ile
ENST00000652415.1:c.157G>A ENSP00000498756.1:p.Val53Ile
ENST00000291532.7:c.157G>A ENSP00000291532.3:p.Val53Ile
ENST00000398397.3:c.157G>A ENSP00000381434.3:p.Val53Ile
ENST00000398405.5:c.151G>A ENSP00000381442.1:p.Val51Ile
ENST00000433957.6:c.157G>A ENSP00000411013.2:p.Val53Ile
ENST00000482761.1:n.444G>A
NM_001256317.1:c.157G>A NP_001243246.1:p.Val53Ile
NM_024022.2:c.157G>A NP_076927.1:p.Val53Ile
NM_032405.1:c.157G>A NP_115781.1:p.Val53Ile
NR_046020.1:n.1113G>A
NM_001256317.2:c.157G>A NP_001243246.1:p.Val53Ile
NM_024022.3:c.157G>A NP_076927.1:p.Val53Ile
NM_032405.2:c.157G>A NP_115781.1:p.Val53Ile
NM_001256317.3:c.157G>A MANE Select NP_001243246.1:p.Val53Ile
NM_024022.4:c.157G>A NP_076927.1:p.Val53Ile