Canonical Allele Identifier: CA410374732
Gene: TMPRSS3 HGNC NCBI

Linked Data

dbSNP Id: rs1229223056

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.42385409C>T , CM000683.2:g.42385409C>T GRCh38
NC_000021.8:g.43805518C>T , CM000683.1:g.43805518C>T GRCh37
NC_000021.7:g.42678587C>T NCBI36
NG_011629.1:g.15683G>A
NG_011629.2:g.15683G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000433957.7:c.572G>A ENSP00000411013.3:p.Arg191Lys
ENST00000644384.2:c.572G>A MANE Select ENSP00000494414.1:p.Arg191Lys
ENST00000652415.1:c.572G>A ENSP00000498756.1:p.Arg191Lys
ENST00000291532.7:c.572G>A ENSP00000291532.3:p.Arg191Lys
ENST00000398397.3:c.572G>A ENSP00000381434.3:p.Arg191Lys
ENST00000398405.5:c.566G>A ENSP00000381442.1:p.Arg189Lys
ENST00000433957.6:c.572G>A ENSP00000411013.2:p.Arg191Lys
ENST00000474596.5:n.440G>A
ENST00000482761.1:n.859G>A
NM_001256317.1:c.572G>A NP_001243246.1:p.Arg191Lys
NM_024022.2:c.572G>A NP_076927.1:p.Arg191Lys
NM_032404.2:c.191G>A NP_115780.1:p.Arg64Lys
NM_032405.1:c.572G>A NP_115781.1:p.Arg191Lys
NR_046020.1:n.1528G>A
NM_001256317.2:c.572G>A NP_001243246.1:p.Arg191Lys
NM_024022.3:c.572G>A NP_076927.1:p.Arg191Lys
NM_032405.2:c.572G>A NP_115781.1:p.Arg191Lys
NM_001256317.3:c.572G>A MANE Select NP_001243246.1:p.Arg191Lys
NM_024022.4:c.572G>A NP_076927.1:p.Arg191Lys
NM_032404.3:c.191G>A NP_115780.1:p.Arg64Lys