Canonical Allele Identifier: CA2390778329

Gene: TMPRSS3

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42382203C= , CM000683.2:g.42382203C=	GRCh38
NC_000021.8:g.43802312C= , CM000683.1:g.43802312C=	GRCh37
NC_000021.7:g.42675381C=	NCBI36
NG_011629.1:g.18889G=
NG_011629.2:g.18889G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433957.7:c.814G=	ENSP00000411013.3:p.Val272=
ENST00000644384.2:c.814G= MANE Select	ENSP00000494414.1:p.Val272=
ENST00000652415.1:c.814G=	ENSP00000498756.1:p.Val272=
ENST00000291532.7:c.814G=	ENSP00000291532.3:p.Val272=
ENST00000398397.3:c.814G=	ENSP00000381434.3:p.Val272=
ENST00000398405.5:c.808G=	ENSP00000381442.1:p.Val270=
ENST00000433957.6:c.814G=	ENSP00000411013.2:p.Val272=
ENST00000474596.5:n.682G=
ENST00000476848.5:n.1549G=
ENST00000478680.1:n.91G=
ENST00000482761.1:n.1101G=
NM_001256317.1:c.814G=	NP_001243246.1:p.Val272=
NM_024022.2:c.814G=	NP_076927.1:p.Val272=
NM_032404.2:c.433G=	NP_115780.1:p.Val145=
NM_032405.1:c.814G=	NP_115781.1:p.Val272=
NR_046020.1:n.1770G=
NM_001256317.2:c.814G=	NP_001243246.1:p.Val272=
NM_024022.3:c.814G=	NP_076927.1:p.Val272=
NM_032405.2:c.814G=	NP_115781.1:p.Val272=
NM_001256317.3:c.814G= MANE Select	NP_001243246.1:p.Val272=
NM_024022.4:c.814G=	NP_076927.1:p.Val272=
NM_032404.3:c.433G=	NP_115780.1:p.Val145=