Canonical Allele Identifier: CA182538

Gene: TMPRSS3

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42380208C>G , CM000683.2:g.42380208C>G	GRCh38
NC_000021.8:g.43800317C>G , CM000683.1:g.43800317C>G	GRCh37
NC_000021.7:g.42673386C>G	NCBI36
NG_011629.1:g.20884G>C
NG_011629.2:g.20884G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433957.7:c.957G>C	ENSP00000411013.3:p.Met319Ile
ENST00000644384.2:c.957G>C MANE Select	ENSP00000494414.1:p.Met319Ile
ENST00000652415.1:c.957G>C	ENSP00000498756.1:p.Met319Ile
ENST00000291532.7:c.957G>C	ENSP00000291532.3:p.Met319Ile
ENST00000398405.5:c.951G>C	ENSP00000381442.1:p.Met317Ile
ENST00000433957.6:c.957G>C	ENSP00000411013.2:p.Met319Ile
ENST00000474596.5:n.825G>C
ENST00000476848.5:n.1692G>C
ENST00000482761.1:n.1244G>C
NM_001256317.1:c.957G>C	NP_001243246.1:p.Met319Ile
NM_024022.2:c.957G>C	NP_076927.1:p.Met319Ile
NM_032404.2:c.576G>C	NP_115780.1:p.Met192Ile
NR_046020.1:n.1913G>C
NM_001256317.2:c.957G>C	NP_001243246.1:p.Met319Ile
NM_024022.3:c.957G>C	NP_076927.1:p.Met319Ile
NM_001256317.3:c.957G>C MANE Select	NP_001243246.1:p.Met319Ile
NM_024022.4:c.957G>C	NP_076927.1:p.Met319Ile
NM_032404.3:c.576G>C	NP_115780.1:p.Met192Ile