Canonical Allele Identifier: CA2390782161

Gene: TMPRSS3

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42389976G= , CM000683.2:g.42389976G=	GRCh38
NC_000021.8:g.43810085G= , CM000683.1:g.43810085G=	GRCh37
NC_000021.7:g.42683154G=	NCBI36
NG_011629.1:g.11116C=
NG_011629.2:g.11116C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433957.7:c.156C=	ENSP00000411013.3:p.Ile52=
ENST00000644384.2:c.156C= MANE Select	ENSP00000494414.1:p.Ile52=
ENST00000652415.1:c.156C=	ENSP00000498756.1:p.Ile52=
ENST00000291532.7:c.156C=	ENSP00000291532.3:p.Ile52=
ENST00000398397.3:c.156C=	ENSP00000381434.3:p.Ile52=
ENST00000398405.5:c.150C=	ENSP00000381442.1:p.Ile50=
ENST00000433957.6:c.156C=	ENSP00000411013.2:p.Ile52=
ENST00000482761.1:n.443C=
NM_001256317.1:c.156C=	NP_001243246.1:p.Ile52=
NM_024022.2:c.156C=	NP_076927.1:p.Ile52=
NM_032405.1:c.156C=	NP_115781.1:p.Ile52=
NR_046020.1:n.1112C=
NM_001256317.2:c.156C=	NP_001243246.1:p.Ile52=
NM_024022.3:c.156C=	NP_076927.1:p.Ile52=
NM_032405.2:c.156C=	NP_115781.1:p.Ile52=
NM_001256317.3:c.156C= MANE Select	NP_001243246.1:p.Ile52=
NM_024022.4:c.156C=	NP_076927.1:p.Ile52=