Canonical Allele Identifier: CA2654678169

Gene: TMPRSS3

Linked Data

• gnomAD v4: 21-42372002-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42372002C>A , CM000683.2:g.42372002C>A	GRCh38
NC_000021.8:g.43792111C>A , CM000683.1:g.43792111C>A	GRCh37
NC_000021.7:g.42665180C>A	NCBI36
NG_011629.1:g.29090G>T
NG_011629.2:g.29090G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433957.7:c.*760G>T	ENSP00000411013.3:n.*760G>T
ENST00000644384.2:c.*760G>T MANE Select	ENSP00000494414.1:n.*760G>T
ENST00000652415.1:c.*760G>T	ENSP00000498756.1:n.*760G>T
ENST00000291532.7:c.*760G>T	ENSP00000291532.3:n.*760G>T
ENST00000398405.5:c.*760G>T	ENSP00000381442.1:n.*760G>T
ENST00000433957.6:c.*760G>T	ENSP00000411013.2:n.*760G>T
ENST00000474596.5:n.1993G>T
ENST00000476848.5:n.2857G>T
ENST00000482761.1:n.2412G>T
NM_001256317.1:c.*760G>T	NP_001243246.1:n.*760G>T
NM_024022.2:c.*760G>T	NP_076927.1:n.*760G>T
NM_032404.2:c.*760G>T	NP_115780.1:n.*760G>T
NR_046020.1:n.3081G>T
NM_001256317.2:c.*760G>T	NP_001243246.1:n.*760G>T
NM_024022.3:c.*760G>T	NP_076927.1:n.*760G>T
NM_001256317.3:c.*760G>T MANE Select	NP_001243246.1:n.*760G>T
NM_024022.4:c.*760G>T	NP_076927.1:n.*760G>T
NM_032404.3:c.*760G>T	NP_115780.1:n.*760G>T