Canonical Allele Identifier: CA2817979416

Gene: TMPRSS3

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42372565A>C , CM000683.2:g.42372565A>C	GRCh38
NC_000021.8:g.43792674A>C , CM000683.1:g.43792674A>C	GRCh37
NC_000021.7:g.42665743A>C	NCBI36
NG_011629.1:g.28527T>G
NG_011629.2:g.28527T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433957.7:c.*197T>G	ENSP00000411013.3:n.*197T>G
ENST00000644384.2:c.*197T>G MANE Select	ENSP00000494414.1:n.*197T>G
ENST00000652415.1:c.*197T>G	ENSP00000498756.1:n.*197T>G
ENST00000291532.7:c.*197T>G	ENSP00000291532.3:n.*197T>G
ENST00000398405.5:c.*197T>G	ENSP00000381442.1:n.*197T>G
ENST00000433957.6:c.*197T>G	ENSP00000411013.2:n.*197T>G
ENST00000474596.5:n.1430T>G
ENST00000476848.5:n.2294T>G
ENST00000482761.1:n.1849T>G
NM_001256317.1:c.*197T>G	NP_001243246.1:n.*197T>G
NM_024022.2:c.*197T>G	NP_076927.1:n.*197T>G
NM_032404.2:c.*197T>G	NP_115780.1:n.*197T>G
NR_046020.1:n.2518T>G
NM_001256317.2:c.*197T>G	NP_001243246.1:n.*197T>G
NM_024022.3:c.*197T>G	NP_076927.1:n.*197T>G
NM_001256317.3:c.*197T>G MANE Select	NP_001243246.1:n.*197T>G
NM_024022.4:c.*197T>G	NP_076927.1:n.*197T>G
NM_032404.3:c.*197T>G	NP_115780.1:n.*197T>G