Canonical Allele Identifier: CA2577612437
Gene: TMPRSS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.42389039_42389040del , CM000683.2:g.42389039_42389040del GRCh38
NC_000021.8:g.43809148_43809149del , CM000683.1:g.43809148_43809149del GRCh37
NC_000021.7:g.42682217_42682218del NCBI36
NG_011629.1:g.12052_12053del
NG_011629.2:g.12052_12053del

Transcript Alleles

HGVS Amino-acid Change
ENST00000433957.7:c.211_212del ENSP00000411013.3:p.Phe71ArgfsTer13
ENST00000644384.2:c.211_212del MANE Select ENSP00000494414.1:p.Phe71ArgfsTer13
ENST00000652415.1:c.211_212del ENSP00000498756.1:p.Phe71ArgfsTer13
ENST00000291532.7:c.211_212del ENSP00000291532.3:p.Phe71ArgfsTer13
ENST00000398397.3:c.211_212del ENSP00000381434.3:p.Phe71ArgfsTer13
ENST00000398405.5:c.205_206del ENSP00000381442.1:p.Phe69ArgfsTer13
ENST00000433957.6:c.211_212del ENSP00000411013.2:p.Phe71ArgfsTer13
ENST00000474596.5:n.79_80del
ENST00000482761.1:n.498_499del
NM_001256317.1:c.211_212del NP_001243246.1:p.Phe71ArgfsTer13
NM_024022.2:c.211_212del NP_076927.1:p.Phe71ArgfsTer13
NM_032404.2:c.-171_-170del NP_115780.1:n.-171_-170del
NM_032405.1:c.211_212del NP_115781.1:p.Phe71ArgfsTer13
NR_046020.1:n.1167_1168del
NM_001256317.2:c.211_212del NP_001243246.1:p.Phe71ArgfsTer13
NM_024022.3:c.211_212del NP_076927.1:p.Phe71ArgfsTer13
NM_032405.2:c.211_212del NP_115781.1:p.Phe71ArgfsTer13
NM_001256317.3:c.211_212del MANE Select NP_001243246.1:p.Phe71ArgfsTer13
NM_024022.4:c.211_212del NP_076927.1:p.Phe71ArgfsTer13
NM_032404.3:c.-171_-170del NP_115780.1:n.-171_-170del