Canonical Allele Identifier: CA2390782159

Gene: TMPRSS3

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42389971A= , CM000683.2:g.42389971A=	GRCh38
NC_000021.8:g.43810080A= , CM000683.1:g.43810080A=	GRCh37
NC_000021.7:g.42683149A=	NCBI36
NG_011629.1:g.11121T=
NG_011629.2:g.11121T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433957.7:c.161T=	ENSP00000411013.3:p.Ile54=
ENST00000644384.2:c.161T= MANE Select	ENSP00000494414.1:p.Ile54=
ENST00000652415.1:c.161T=	ENSP00000498756.1:p.Ile54=
ENST00000291532.7:c.161T=	ENSP00000291532.3:p.Ile54=
ENST00000398397.3:c.161T=	ENSP00000381434.3:p.Ile54=
ENST00000398405.5:c.155T=	ENSP00000381442.1:p.Ile52=
ENST00000433957.6:c.161T=	ENSP00000411013.2:p.Ile54=
ENST00000482761.1:n.448T=
NM_001256317.1:c.161T=	NP_001243246.1:p.Ile54=
NM_024022.2:c.161T=	NP_076927.1:p.Ile54=
NM_032405.1:c.161T=	NP_115781.1:p.Ile54=
NR_046020.1:n.1117T=
NM_001256317.2:c.161T=	NP_001243246.1:p.Ile54=
NM_024022.3:c.161T=	NP_076927.1:p.Ile54=
NM_032405.2:c.161T=	NP_115781.1:p.Ile54=
NM_001256317.3:c.161T= MANE Select	NP_001243246.1:p.Ile54=
NM_024022.4:c.161T=	NP_076927.1:p.Ile54=