Canonical Allele Identifier: CA2390778167

Gene: TMPRSS3

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42381928A= , CM000683.2:g.42381928A=	GRCh38
NC_000021.8:g.43802037A= , CM000683.1:g.43802037A=	GRCh37
NC_000021.7:g.42675106A=	NCBI36
NG_011629.1:g.19164T=
NG_011629.2:g.19164T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433957.7:c.952+137T=	ENSP00000411013.3:n.952+137T=
ENST00000644384.2:c.952+137T= MANE Select	ENSP00000494414.1:n.952+137T=
ENST00000652415.1:c.952+137T=	ENSP00000498756.1:n.952+137T=
ENST00000291532.7:c.952+137T=	ENSP00000291532.3:n.952+137T=
ENST00000398397.3:c.*54T=	ENSP00000381434.3:n.*54T=
ENST00000398405.5:c.946+137T=	ENSP00000381442.1:n.946+137T=
ENST00000433957.6:c.952+137T=	ENSP00000411013.2:n.952+137T=
ENST00000474596.5:n.820+137T=
ENST00000476848.5:n.1687+137T=
ENST00000478680.1:n.366T=
ENST00000482761.1:n.1239+137T=
NM_001256317.1:c.952+137T=	NP_001243246.1:n.952+137T=
NM_024022.2:c.952+137T=	NP_076927.1:n.952+137T=
NM_032404.2:c.571+137T=	NP_115780.1:n.571+137T=
NM_032405.1:c.*54T=	NP_115781.1:n.*54T=
NR_046020.1:n.1908+137T=
NM_001256317.2:c.952+137T=	NP_001243246.1:n.952+137T=
NM_024022.3:c.952+137T=	NP_076927.1:n.952+137T=
NM_032405.2:c.*54T=	NP_115781.1:n.*54T=
NM_001256317.3:c.952+137T= MANE Select	NP_001243246.1:n.952+137T=
NM_024022.4:c.952+137T=	NP_076927.1:n.952+137T=
NM_032404.3:c.571+137T=	NP_115780.1:n.571+137T=