Canonical Allele Identifier: CA2390778347

Gene: TMPRSS3

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42382221T= , CM000683.2:g.42382221T=	GRCh38
NC_000021.8:g.43802330T= , CM000683.1:g.43802330T=	GRCh37
NC_000021.7:g.42675399T=	NCBI36
NG_011629.1:g.18871A=
NG_011629.2:g.18871A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433957.7:c.796A=	ENSP00000411013.3:p.Lys266=
ENST00000644384.2:c.796A= MANE Select	ENSP00000494414.1:p.Lys266=
ENST00000652415.1:c.796A=	ENSP00000498756.1:p.Lys266=
ENST00000291532.7:c.796A=	ENSP00000291532.3:p.Lys266=
ENST00000398397.3:c.796A=	ENSP00000381434.3:p.Lys266=
ENST00000398405.5:c.790A=	ENSP00000381442.1:p.Lys264=
ENST00000433957.6:c.796A=	ENSP00000411013.2:p.Lys266=
ENST00000474596.5:n.664A=
ENST00000476848.5:n.1531A=
ENST00000478680.1:n.73A=
ENST00000482761.1:n.1083A=
NM_001256317.1:c.796A=	NP_001243246.1:p.Lys266=
NM_024022.2:c.796A=	NP_076927.1:p.Lys266=
NM_032404.2:c.415A=	NP_115780.1:p.Lys139=
NM_032405.1:c.796A=	NP_115781.1:p.Lys266=
NR_046020.1:n.1752A=
NM_001256317.2:c.796A=	NP_001243246.1:p.Lys266=
NM_024022.3:c.796A=	NP_076927.1:p.Lys266=
NM_032405.2:c.796A=	NP_115781.1:p.Lys266=
NM_001256317.3:c.796A= MANE Select	NP_001243246.1:p.Lys266=
NM_024022.4:c.796A=	NP_076927.1:p.Lys266=
NM_032404.3:c.415A=	NP_115780.1:p.Lys139=