Canonical Allele Identifier: CA2390781698
Gene: TMPRSS3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000021.9:g.42389025T= , CM000683.2:g.42389025T= GRCh38
NC_000021.8:g.43809134T= , CM000683.1:g.43809134T= GRCh37
NC_000021.7:g.42682203T= NCBI36
NG_011629.1:g.12067A=
NG_011629.2:g.12067A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000433957.7:c.226A= ENSP00000411013.3:p.Lys76=
ENST00000644384.2:c.226A= MANE Select ENSP00000494414.1:p.Lys76=
ENST00000652415.1:c.226A= ENSP00000498756.1:p.Lys76=
ENST00000291532.7:c.226A= ENSP00000291532.3:p.Lys76=
ENST00000398397.3:c.226A= ENSP00000381434.3:p.Lys76=
ENST00000398405.5:c.220A= ENSP00000381442.1:p.Lys74=
ENST00000433957.6:c.226A= ENSP00000411013.2:p.Lys76=
ENST00000474596.5:n.94A=
ENST00000482761.1:n.513A=
NM_001256317.1:c.226A= NP_001243246.1:p.Lys76=
NM_024022.2:c.226A= NP_076927.1:p.Lys76=
NM_032404.2:c.-156A= NP_115780.1:n.-156A=
NM_032405.1:c.226A= NP_115781.1:p.Lys76=
NR_046020.1:n.1182A=
NM_001256317.2:c.226A= NP_001243246.1:p.Lys76=
NM_024022.3:c.226A= NP_076927.1:p.Lys76=
NM_032405.2:c.226A= NP_115781.1:p.Lys76=
NM_001256317.3:c.226A= MANE Select NP_001243246.1:p.Lys76=
NM_024022.4:c.226A= NP_076927.1:p.Lys76=
NM_032404.3:c.-156A= NP_115780.1:n.-156A=