Canonical Allele Identifier: CA2654679455

Gene: TMPRSS3

Linked Data

• gnomAD v4: 21-42382422-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42382426del , CM000683.2:g.42382426del	GRCh38
NC_000021.8:g.43802535del , CM000683.1:g.43802535del	GRCh37
NC_000021.7:g.42675604del	NCBI36
NG_011629.1:g.18669del
NG_011629.2:g.18669del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433957.7:c.783-189del	ENSP00000411013.3:n.783-189del
ENST00000644384.2:c.783-189del MANE Select	ENSP00000494414.1:n.783-189del
ENST00000652415.1:c.783-189del	ENSP00000498756.1:n.783-189del
ENST00000291532.7:c.783-189del	ENSP00000291532.3:n.783-189del
ENST00000398397.3:c.783-189del	ENSP00000381434.3:n.783-189del
ENST00000398405.5:c.777-189del	ENSP00000381442.1:n.777-189del
ENST00000433957.6:c.783-189del	ENSP00000411013.2:n.783-189del
ENST00000474596.5:n.651-189del
ENST00000476848.5:n.1329del
ENST00000478680.1:n.60-189del
ENST00000482761.1:n.1070-189del
NM_001256317.1:c.783-189del	NP_001243246.1:n.783-189del
NM_024022.2:c.783-189del	NP_076927.1:n.783-189del
NM_032404.2:c.402-189del	NP_115780.1:n.402-189del
NM_032405.1:c.783-189del	NP_115781.1:n.783-189del
NR_046020.1:n.1739-189del
NM_001256317.2:c.783-189del	NP_001243246.1:n.783-189del
NM_024022.3:c.783-189del	NP_076927.1:n.783-189del
NM_032405.2:c.783-189del	NP_115781.1:n.783-189del
NM_001256317.3:c.783-189del MANE Select	NP_001243246.1:n.783-189del
NM_024022.4:c.783-189del	NP_076927.1:n.783-189del
NM_032404.3:c.402-189del	NP_115780.1:n.402-189del