Canonical Allele Identifier: CA410375179
Gene: TMPRSS3 HGNC NCBI

Linked Data

dbSNP Id: rs2052619127

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.42385493C>T , CM000683.2:g.42385493C>T GRCh38
NC_000021.8:g.43805602C>T , CM000683.1:g.43805602C>T GRCh37
NC_000021.7:g.42678671C>T NCBI36
NG_011629.1:g.15599G>A
NG_011629.2:g.15599G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000433957.7:c.488G>A ENSP00000411013.3:p.Gly163Glu
ENST00000644384.2:c.488G>A MANE Select ENSP00000494414.1:p.Gly163Glu
ENST00000652415.1:c.488G>A ENSP00000498756.1:p.Gly163Glu
ENST00000291532.7:c.488G>A ENSP00000291532.3:p.Gly163Glu
ENST00000398397.3:c.488G>A ENSP00000381434.3:p.Gly163Glu
ENST00000398405.5:c.482G>A ENSP00000381442.1:p.Gly161Glu
ENST00000433957.6:c.488G>A ENSP00000411013.2:p.Gly163Glu
ENST00000474596.5:n.356G>A
ENST00000482761.1:n.775G>A
NM_001256317.1:c.488G>A NP_001243246.1:p.Gly163Glu
NM_024022.2:c.488G>A NP_076927.1:p.Gly163Glu
NM_032404.2:c.107G>A NP_115780.1:p.Gly36Glu
NM_032405.1:c.488G>A NP_115781.1:p.Gly163Glu
NR_046020.1:n.1444G>A
NM_001256317.2:c.488G>A NP_001243246.1:p.Gly163Glu
NM_024022.3:c.488G>A NP_076927.1:p.Gly163Glu
NM_032405.2:c.488G>A NP_115781.1:p.Gly163Glu
NM_001256317.3:c.488G>A MANE Select NP_001243246.1:p.Gly163Glu
NM_024022.4:c.488G>A NP_076927.1:p.Gly163Glu
NM_032404.3:c.107G>A NP_115780.1:p.Gly36Glu