Canonical Allele Identifier: CA2390781638
Gene: TMPRSS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.42388909G= , CM000683.2:g.42388909G= GRCh38
NC_000021.8:g.43809018G= , CM000683.1:g.43809018G= GRCh37
NC_000021.7:g.42682087G= NCBI36
NG_011629.1:g.12183C=
NG_011629.2:g.12183C=

Transcript Alleles

HGVS Amino-acid change
ENST00000433957.7:c.322+20C= ENSP00000411013.3:n.322+20C=
ENST00000644384.2:c.322+20C= MANE Select ENSP00000494414.1:n.322+20C=
ENST00000652415.1:c.322+20C= ENSP00000498756.1:n.322+20C=
ENST00000291532.7:c.322+20C= ENSP00000291532.3:n.322+20C=
ENST00000398397.3:c.322+20C= ENSP00000381434.3:n.322+20C=
ENST00000398405.5:c.316+20C= ENSP00000381442.1:n.316+20C=
ENST00000433957.6:c.322+20C= ENSP00000411013.2:n.322+20C=
ENST00000474596.5:n.190+20C=
ENST00000482761.1:n.609+20C=
NM_001256317.1:c.322+20C= NP_001243246.1:n.322+20C=
NM_024022.2:c.322+20C= NP_076927.1:n.322+20C=
NM_032404.2:c.-60+20C= NP_115780.1:n.-60+20C=
NM_032405.1:c.322+20C= NP_115781.1:n.322+20C=
NR_046020.1:n.1278+20C=
NM_001256317.2:c.322+20C= NP_001243246.1:n.322+20C=
NM_024022.3:c.322+20C= NP_076927.1:n.322+20C=
NM_032405.2:c.322+20C= NP_115781.1:n.322+20C=
NM_001256317.3:c.322+20C= MANE Select NP_001243246.1:n.322+20C=
NM_024022.4:c.322+20C= NP_076927.1:n.322+20C=
NM_032404.3:c.-60+20C= NP_115780.1:n.-60+20C=