Canonical Allele Identifier: CA3241877854

Gene: TMPRSS3

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42384007T= , CM000683.2:g.42384007T=	GRCh38
NC_000021.8:g.43804116T= , CM000683.1:g.43804116T=	GRCh37
NC_000021.7:g.42677185T=	NCBI36
NG_011629.1:g.17085A=
NG_011629.2:g.17085A=

Transcript Alleles

HGVS	Amino-acid Change
NM_001256317.3:c.579A= MANE Select	NP_001243246.1:p.Gly193=
ENST00000644384.2:c.579A= MANE Select	ENSP00000494414.1:p.Gly193=
NM_001256317.1:c.579A=	NP_001243246.1:p.Gly193=
NM_001256317.2:c.579A=	NP_001243246.1:p.Gly193=
NM_024022.2:c.579A=	NP_076927.1:p.Gly193=
NM_024022.3:c.579A=	NP_076927.1:p.Gly193=
NM_024022.4:c.579A=	NP_076927.1:p.Gly193=
NM_032404.2:c.198A=	NP_115780.1:p.Gly66=
NM_032404.3:c.198A=	NP_115780.1:p.Gly66=
NM_032405.1:c.579A=	NP_115781.1:p.Gly193=
NM_032405.2:c.579A=	NP_115781.1:p.Gly193=
NR_046020.1:n.1535A=
ENST00000291532.7:c.579A=	ENSP00000291532.3:p.Gly193=
ENST00000398397.3:c.579A=	ENSP00000381434.3:p.Gly193=
ENST00000398405.5:c.573A=	ENSP00000381442.1:p.Gly191=
ENST00000433957.6:c.579A=	ENSP00000411013.2:p.Gly193=
ENST00000433957.7:c.579A=	ENSP00000411013.3:p.Gly193=
ENST00000474596.5:n.447A=
ENST00000482761.1:n.866A=
ENST00000652415.1:c.579A=	ENSP00000498756.1:p.Gly193=