Canonical Allele Identifier: CA2654679334

Gene: TMPRSS3

Linked Data

• gnomAD v4: 21-42381947-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42381947A>T , CM000683.2:g.42381947A>T	GRCh38
NC_000021.8:g.43802056A>T , CM000683.1:g.43802056A>T	GRCh37
NC_000021.7:g.42675125A>T	NCBI36
NG_011629.1:g.19145T>A
NG_011629.2:g.19145T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433957.7:c.952+118T>A	ENSP00000411013.3:n.952+118T>A
ENST00000644384.2:c.952+118T>A MANE Select	ENSP00000494414.1:n.952+118T>A
ENST00000652415.1:c.952+118T>A	ENSP00000498756.1:n.952+118T>A
ENST00000291532.7:c.952+118T>A	ENSP00000291532.3:n.952+118T>A
ENST00000398397.3:c.*35T>A	ENSP00000381434.3:n.*35T>A
ENST00000398405.5:c.946+118T>A	ENSP00000381442.1:n.946+118T>A
ENST00000433957.6:c.952+118T>A	ENSP00000411013.2:n.952+118T>A
ENST00000474596.5:n.820+118T>A
ENST00000476848.5:n.1687+118T>A
ENST00000478680.1:n.347T>A
ENST00000482761.1:n.1239+118T>A
NM_001256317.1:c.952+118T>A	NP_001243246.1:n.952+118T>A
NM_024022.2:c.952+118T>A	NP_076927.1:n.952+118T>A
NM_032404.2:c.571+118T>A	NP_115780.1:n.571+118T>A
NM_032405.1:c.*35T>A	NP_115781.1:n.*35T>A
NR_046020.1:n.1908+118T>A
NM_001256317.2:c.952+118T>A	NP_001243246.1:n.952+118T>A
NM_024022.3:c.952+118T>A	NP_076927.1:n.952+118T>A
NM_032405.2:c.*35T>A	NP_115781.1:n.*35T>A
NM_001256317.3:c.952+118T>A MANE Select	NP_001243246.1:n.952+118T>A
NM_024022.4:c.952+118T>A	NP_076927.1:n.952+118T>A
NM_032404.3:c.571+118T>A	NP_115780.1:n.571+118T>A