Canonical Allele Identifier: CA321548638
Community Standard Title: NM_001256317.3(TMPRSS3):c.322+161del
Gene: TMPRSS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.42388773del , CM000683.2:g.42388773del GRCh38
NC_000021.8:g.43808882del , CM000683.1:g.43808882del GRCh37
NC_000021.7:g.42681951del NCBI36
NG_011629.1:g.12324del
NG_011629.2:g.12324del

Transcript Alleles

HGVS Amino-acid Change
NM_001256317.3:c.322+161del MANE Select NP_001243246.1:n.322+161del
ENST00000644384.2:c.322+161del MANE Select ENSP00000494414.1:n.322+161del
NM_001256317.1:c.322+161del NP_001243246.1:n.322+161del
NM_001256317.2:c.322+161del NP_001243246.1:n.322+161del
NM_024022.2:c.322+161del NP_076927.1:n.322+161del
NM_024022.3:c.322+161del NP_076927.1:n.322+161del
NM_024022.4:c.322+161del NP_076927.1:n.322+161del
NM_032404.2:c.-60+161del NP_115780.1:n.-60+161del
NM_032404.3:c.-60+161del NP_115780.1:n.-60+161del
NM_032405.1:c.322+161del NP_115781.1:n.322+161del
NM_032405.2:c.322+161del NP_115781.1:n.322+161del
NR_046020.1:n.1278+161del
ENST00000291532.7:c.322+161del ENSP00000291532.3:n.322+161del
ENST00000398397.3:c.322+161del ENSP00000381434.3:n.322+161del
ENST00000398405.5:c.316+161del ENSP00000381442.1:n.316+161del
ENST00000433957.6:c.322+161del ENSP00000411013.2:n.322+161del
ENST00000433957.7:c.322+161del ENSP00000411013.3:n.322+161del
ENST00000474596.5:n.190+161del
ENST00000482761.1:n.609+161del
ENST00000652415.1:c.322+161del ENSP00000498756.1:n.322+161del