Canonical Allele Identifier: CA2390775261

Gene: TMPRSS3

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42375852G= , CM000683.2:g.42375852G=	GRCh38
NC_000021.8:g.43795961G= , CM000683.1:g.43795961G=	GRCh37
NC_000021.7:g.42669030G=	NCBI36
NG_011629.1:g.25240C=
NG_011629.2:g.25240C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001256317.3:c.1208C= MANE Select	NP_001243246.1:p.Pro403=
ENST00000644384.2:c.1208C= MANE Select	ENSP00000494414.1:p.Pro403=
NM_001256317.1:c.1208C=	NP_001243246.1:p.Pro403=
NM_001256317.2:c.1208C=	NP_001243246.1:p.Pro403=
NM_024022.2:c.1211C=	NP_076927.1:p.Pro404=
NM_024022.3:c.1211C=	NP_076927.1:p.Pro404=
NM_024022.4:c.1211C=	NP_076927.1:p.Pro404=
NM_032404.2:c.830C=	NP_115780.1:p.Pro277=
NM_032404.3:c.830C=	NP_115780.1:p.Pro277=
NR_046020.1:n.2167C=
ENST00000291532.7:c.1211C=	ENSP00000291532.3:p.Pro404=
ENST00000398405.5:c.1202C=	ENSP00000381442.1:p.Pro401=
ENST00000433957.6:c.1208C=	ENSP00000411013.2:p.Pro403=
ENST00000433957.7:c.1211C=	ENSP00000411013.3:p.Pro404=
ENST00000474596.5:n.1079C=
ENST00000476848.5:n.1943C=
ENST00000482761.1:n.1498C=
ENST00000652415.1:c.1208C=	ENSP00000498756.1:p.Pro403=