Canonical Allele Identifier: CA2390778343

Gene: TMPRSS3

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42382217G= , CM000683.2:g.42382217G=	GRCh38
NC_000021.8:g.43802326G= , CM000683.1:g.43802326G=	GRCh37
NC_000021.7:g.42675395G=	NCBI36
NG_011629.1:g.18875C=
NG_011629.2:g.18875C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433957.7:c.800C=	ENSP00000411013.3:p.Ser267=
ENST00000644384.2:c.800C= MANE Select	ENSP00000494414.1:p.Ser267=
ENST00000652415.1:c.800C=	ENSP00000498756.1:p.Ser267=
ENST00000291532.7:c.800C=	ENSP00000291532.3:p.Ser267=
ENST00000398397.3:c.800C=	ENSP00000381434.3:p.Ser267=
ENST00000398405.5:c.794C=	ENSP00000381442.1:p.Ser265=
ENST00000433957.6:c.800C=	ENSP00000411013.2:p.Ser267=
ENST00000474596.5:n.668C=
ENST00000476848.5:n.1535C=
ENST00000478680.1:n.77C=
ENST00000482761.1:n.1087C=
NM_001256317.1:c.800C=	NP_001243246.1:p.Ser267=
NM_024022.2:c.800C=	NP_076927.1:p.Ser267=
NM_032404.2:c.419C=	NP_115780.1:p.Ser140=
NM_032405.1:c.800C=	NP_115781.1:p.Ser267=
NR_046020.1:n.1756C=
NM_001256317.2:c.800C=	NP_001243246.1:p.Ser267=
NM_024022.3:c.800C=	NP_076927.1:p.Ser267=
NM_032405.2:c.800C=	NP_115781.1:p.Ser267=
NM_001256317.3:c.800C= MANE Select	NP_001243246.1:p.Ser267=
NM_024022.4:c.800C=	NP_076927.1:p.Ser267=
NM_032404.3:c.419C=	NP_115780.1:p.Ser140=