Canonical Allele Identifier: CA2390773412

Gene: TMPRSS3

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42372413A= , CM000683.2:g.42372413A=	GRCh38
NC_000021.8:g.43792522A= , CM000683.1:g.43792522A=	GRCh37
NC_000021.7:g.42665591A=	NCBI36
NG_011629.1:g.28679T=
NG_011629.2:g.28679T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000433957.7:c.*349T=	ENSP00000411013.3:n.*349T=
ENST00000644384.2:c.*349T= MANE Select	ENSP00000494414.1:n.*349T=
ENST00000652415.1:c.*349T=	ENSP00000498756.1:n.*349T=
ENST00000291532.7:c.*349T=	ENSP00000291532.3:n.*349T=
ENST00000398405.5:c.*349T=	ENSP00000381442.1:n.*349T=
ENST00000433957.6:c.*349T=	ENSP00000411013.2:n.*349T=
ENST00000474596.5:n.1582T=
ENST00000476848.5:n.2446T=
ENST00000482761.1:n.2001T=
NM_001256317.1:c.*349T=	NP_001243246.1:n.*349T=
NM_024022.2:c.*349T=	NP_076927.1:n.*349T=
NM_032404.2:c.*349T=	NP_115780.1:n.*349T=
NR_046020.1:n.2670T=
NM_001256317.2:c.*349T=	NP_001243246.1:n.*349T=
NM_024022.3:c.*349T=	NP_076927.1:n.*349T=
NM_001256317.3:c.*349T= MANE Select	NP_001243246.1:n.*349T=
NM_024022.4:c.*349T=	NP_076927.1:n.*349T=
NM_032404.3:c.*349T=	NP_115780.1:n.*349T=