Canonical Allele Identifier: CA2390773436

Gene: TMPRSS3

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42372477T= , CM000683.2:g.42372477T=	GRCh38
NC_000021.8:g.43792586T= , CM000683.1:g.43792586T=	GRCh37
NC_000021.7:g.42665655T=	NCBI36
NG_011629.1:g.28615A=
NG_011629.2:g.28615A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000433957.7:c.*285A=	ENSP00000411013.3:n.*285A=
ENST00000644384.2:c.*285A= MANE Select	ENSP00000494414.1:n.*285A=
ENST00000652415.1:c.*285A=	ENSP00000498756.1:n.*285A=
ENST00000291532.7:c.*285A=	ENSP00000291532.3:n.*285A=
ENST00000398405.5:c.*285A=	ENSP00000381442.1:n.*285A=
ENST00000433957.6:c.*285A=	ENSP00000411013.2:n.*285A=
ENST00000474596.5:n.1518A=
ENST00000476848.5:n.2382A=
ENST00000482761.1:n.1937A=
NM_001256317.1:c.*285A=	NP_001243246.1:n.*285A=
NM_024022.2:c.*285A=	NP_076927.1:n.*285A=
NM_032404.2:c.*285A=	NP_115780.1:n.*285A=
NR_046020.1:n.2606A=
NM_001256317.2:c.*285A=	NP_001243246.1:n.*285A=
NM_024022.3:c.*285A=	NP_076927.1:n.*285A=
NM_001256317.3:c.*285A= MANE Select	NP_001243246.1:n.*285A=
NM_024022.4:c.*285A=	NP_076927.1:n.*285A=
NM_032404.3:c.*285A=	NP_115780.1:n.*285A=