Canonical Allele Identifier: CA10042496

Gene: TMPRSS3

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42383134C>T , CM000683.2:g.42383134C>T	GRCh38
NC_000021.8:g.43803243C>T , CM000683.1:g.43803243C>T	GRCh37
NC_000021.7:g.42676312C>T	NCBI36
NG_011629.1:g.17958G>A
NG_011629.2:g.17958G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433957.7:c.681G>A	ENSP00000411013.3:p.Gln227=
ENST00000644384.2:c.681G>A MANE Select	ENSP00000494414.1:p.Gln227=
ENST00000652415.1:c.681G>A	ENSP00000498756.1:p.Gln227=
ENST00000291532.7:c.681G>A	ENSP00000291532.3:p.Gln227=
ENST00000398397.3:c.681G>A	ENSP00000381434.3:p.Gln227=
ENST00000398405.5:c.675G>A	ENSP00000381442.1:p.Gln225=
ENST00000433957.6:c.681G>A	ENSP00000411013.2:p.Gln227=
ENST00000474596.5:n.549G>A
ENST00000476848.5:n.618G>A
ENST00000482761.1:n.968G>A
NM_001256317.1:c.681G>A	NP_001243246.1:p.Gln227=
NM_024022.2:c.681G>A	NP_076927.1:p.Gln227=
NM_032404.2:c.300G>A	NP_115780.1:p.Gln100=
NM_032405.1:c.681G>A	NP_115781.1:p.Gln227=
NR_046020.1:n.1637G>A
NM_001256317.2:c.681G>A	NP_001243246.1:p.Gln227=
NM_024022.3:c.681G>A	NP_076927.1:p.Gln227=
NM_032405.2:c.681G>A	NP_115781.1:p.Gln227=
NM_001256317.3:c.681G>A MANE Select	NP_001243246.1:p.Gln227=
NM_024022.4:c.681G>A	NP_076927.1:p.Gln227=
NM_032404.3:c.300G>A	NP_115780.1:p.Gln100=