Canonical Allele Identifier: CA2390779902

Gene: TMPRSS3

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42385484C= , CM000683.2:g.42385484C=	GRCh38
NC_000021.8:g.43805593C= , CM000683.1:g.43805593C=	GRCh37
NC_000021.7:g.42678662C=	NCBI36
NG_011629.1:g.15608G=
NG_011629.2:g.15608G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000433957.7:c.497G=	ENSP00000411013.3:p.Arg166=
ENST00000644384.2:c.497G= MANE Select	ENSP00000494414.1:p.Arg166=
ENST00000652415.1:c.497G=	ENSP00000498756.1:p.Arg166=
ENST00000291532.7:c.497G=	ENSP00000291532.3:p.Arg166=
ENST00000398397.3:c.497G=	ENSP00000381434.3:p.Arg166=
ENST00000398405.5:c.491G=	ENSP00000381442.1:p.Arg164=
ENST00000433957.6:c.497G=	ENSP00000411013.2:p.Arg166=
ENST00000474596.5:n.365G=
ENST00000482761.1:n.784G=
NM_001256317.1:c.497G=	NP_001243246.1:p.Arg166=
NM_024022.2:c.497G=	NP_076927.1:p.Arg166=
NM_032404.2:c.116G=	NP_115780.1:p.Arg39=
NM_032405.1:c.497G=	NP_115781.1:p.Arg166=
NR_046020.1:n.1453G=
NM_001256317.2:c.497G=	NP_001243246.1:p.Arg166=
NM_024022.3:c.497G=	NP_076927.1:p.Arg166=
NM_032405.2:c.497G=	NP_115781.1:p.Arg166=
NM_001256317.3:c.497G= MANE Select	NP_001243246.1:p.Arg166=
NM_024022.4:c.497G=	NP_076927.1:p.Arg166=
NM_032404.3:c.116G=	NP_115780.1:p.Arg39=