Canonical Allele Identifier: CA2654678167

Gene: TMPRSS3

Linked Data

• gnomAD v4: 21-42371979-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42371979A>C , CM000683.2:g.42371979A>C	GRCh38
NC_000021.8:g.43792088A>C , CM000683.1:g.43792088A>C	GRCh37
NC_000021.7:g.42665157A>C	NCBI36
NG_011629.1:g.29113T>G
NG_011629.2:g.29113T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433957.7:c.*783T>G	ENSP00000411013.3:n.*783T>G
ENST00000644384.2:c.*783T>G MANE Select	ENSP00000494414.1:n.*783T>G
ENST00000652415.1:c.*783T>G	ENSP00000498756.1:n.*783T>G
ENST00000291532.7:c.*783T>G	ENSP00000291532.3:n.*783T>G
ENST00000398405.5:c.*783T>G	ENSP00000381442.1:n.*783T>G
ENST00000433957.6:c.*783T>G	ENSP00000411013.2:n.*783T>G
ENST00000474596.5:n.2016T>G
ENST00000476848.5:n.2880T>G
ENST00000482761.1:n.2435T>G
NM_001256317.1:c.*783T>G	NP_001243246.1:n.*783T>G
NM_024022.2:c.*783T>G	NP_076927.1:n.*783T>G
NM_032404.2:c.*783T>G	NP_115780.1:n.*783T>G
NR_046020.1:n.3104T>G
NM_001256317.2:c.*783T>G	NP_001243246.1:n.*783T>G
NM_024022.3:c.*783T>G	NP_076927.1:n.*783T>G
NM_001256317.3:c.*783T>G MANE Select	NP_001243246.1:n.*783T>G
NM_024022.4:c.*783T>G	NP_076927.1:n.*783T>G
NM_032404.3:c.*783T>G	NP_115780.1:n.*783T>G