Canonical Allele Identifier: CA2390778361

Gene: TMPRSS3

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42382234G= , CM000683.2:g.42382234G=	GRCh38
NC_000021.8:g.43802343G= , CM000683.1:g.43802343G=	GRCh37
NC_000021.7:g.42675412G=	NCBI36
NG_011629.1:g.18858C=
NG_011629.2:g.18858C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433957.7:c.783C=	ENSP00000411013.3:p.Asp261=
ENST00000644384.2:c.783C= MANE Select	ENSP00000494414.1:p.Asp261=
ENST00000652415.1:c.783C=	ENSP00000498756.1:p.Asp261=
ENST00000291532.7:c.783C=	ENSP00000291532.3:p.Asp261=
ENST00000398397.3:c.783C=	ENSP00000381434.3:p.Asp261=
ENST00000398405.5:c.777C=	ENSP00000381442.1:p.Asp259=
ENST00000433957.6:c.783C=	ENSP00000411013.2:p.Asp261=
ENST00000474596.5:n.651C=
ENST00000476848.5:n.1518C=
ENST00000478680.1:n.60C=
ENST00000482761.1:n.1070C=
NM_001256317.1:c.783C=	NP_001243246.1:p.Asp261=
NM_024022.2:c.783C=	NP_076927.1:p.Asp261=
NM_032404.2:c.402C=	NP_115780.1:p.Asp134=
NM_032405.1:c.783C=	NP_115781.1:p.Asp261=
NR_046020.1:n.1739C=
NM_001256317.2:c.783C=	NP_001243246.1:p.Asp261=
NM_024022.3:c.783C=	NP_076927.1:p.Asp261=
NM_032405.2:c.783C=	NP_115781.1:p.Asp261=
NM_001256317.3:c.783C= MANE Select	NP_001243246.1:p.Asp261=
NM_024022.4:c.783C=	NP_076927.1:p.Asp261=
NM_032404.3:c.402C=	NP_115780.1:p.Asp134=