Canonical Allele Identifier: CA657663049

Gene: TMPRSS3

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42372557dup , CM000683.2:g.42372557dup	GRCh38
NC_000021.8:g.43792666dup , CM000683.1:g.43792666dup	GRCh37
NC_000021.7:g.42665735dup	NCBI36
NG_011629.1:g.28535dup
NG_011629.2:g.28535dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433957.7:c.*205dup	ENSP00000411013.3:n.*205dup
ENST00000644384.2:c.*205dup MANE Select	ENSP00000494414.1:n.*205dup
ENST00000652415.1:c.*205dup	ENSP00000498756.1:n.*205dup
ENST00000291532.7:c.*205dup	ENSP00000291532.3:n.*205dup
ENST00000398405.5:c.*205dup	ENSP00000381442.1:n.*205dup
ENST00000433957.6:c.*205dup	ENSP00000411013.2:n.*205dup
ENST00000474596.5:n.1438dup
ENST00000476848.5:n.2302dup
ENST00000482761.1:n.1857dup
NM_001256317.1:c.*205dup	NP_001243246.1:n.*205dup
NM_024022.2:c.*205dup	NP_076927.1:n.*205dup
NM_032404.2:c.*205dup	NP_115780.1:n.*205dup
NR_046020.1:n.2526dup
NM_001256317.2:c.*205dup	NP_001243246.1:n.*205dup
NM_024022.3:c.*205dup	NP_076927.1:n.*205dup
NM_001256317.3:c.*205dup MANE Select	NP_001243246.1:n.*205dup
NM_024022.4:c.*205dup	NP_076927.1:n.*205dup
NM_032404.3:c.*205dup	NP_115780.1:n.*205dup