Canonical Allele Identifier: CA2390773447

Gene: TMPRSS3

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42372496G= , CM000683.2:g.42372496G=	GRCh38
NC_000021.8:g.43792605G= , CM000683.1:g.43792605G=	GRCh37
NC_000021.7:g.42665674G=	NCBI36
NG_011629.1:g.28596C=
NG_011629.2:g.28596C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433957.7:c.*266C=	ENSP00000411013.3:n.*266C=
ENST00000644384.2:c.*266C= MANE Select	ENSP00000494414.1:n.*266C=
ENST00000652415.1:c.*266C=	ENSP00000498756.1:n.*266C=
ENST00000291532.7:c.*266C=	ENSP00000291532.3:n.*266C=
ENST00000398405.5:c.*266C=	ENSP00000381442.1:n.*266C=
ENST00000433957.6:c.*266C=	ENSP00000411013.2:n.*266C=
ENST00000474596.5:n.1499C=
ENST00000476848.5:n.2363C=
ENST00000482761.1:n.1918C=
NM_001256317.1:c.*266C=	NP_001243246.1:n.*266C=
NM_024022.2:c.*266C=	NP_076927.1:n.*266C=
NM_032404.2:c.*266C=	NP_115780.1:n.*266C=
NR_046020.1:n.2587C=
NM_001256317.2:c.*266C=	NP_001243246.1:n.*266C=
NM_024022.3:c.*266C=	NP_076927.1:n.*266C=
NM_001256317.3:c.*266C= MANE Select	NP_001243246.1:n.*266C=
NM_024022.4:c.*266C=	NP_076927.1:n.*266C=
NM_032404.3:c.*266C=	NP_115780.1:n.*266C=