Canonical Allele Identifier: CA410376022

Gene: TMPRSS3

Linked Data

• dbSNP Id: rs1421236349
• gnomAD v2: 21-43810137-G-A
• gnomAD v4: 21-42390028-G-A
• MyVariant Identifiers: chr21:g.43810137G>A (hg19) ; chr21:g.42390028G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42390028G>A , CM000683.2:g.42390028G>A	GRCh38
NC_000021.8:g.43810137G>A , CM000683.1:g.43810137G>A	GRCh37
NC_000021.7:g.42683206G>A	NCBI36
NG_011629.1:g.11064C>T
NG_011629.2:g.11064C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433957.7:c.104C>T	ENSP00000411013.3:p.Ala35Val
ENST00000644384.2:c.104C>T MANE Select	ENSP00000494414.1:p.Ala35Val
ENST00000652415.1:c.104C>T	ENSP00000498756.1:p.Ala35Val
ENST00000291532.7:c.104C>T	ENSP00000291532.3:p.Ala35Val
ENST00000398397.3:c.104C>T	ENSP00000381434.3:p.Ala35Val
ENST00000398405.5:c.98C>T	ENSP00000381442.1:p.Ala33Val
ENST00000433957.6:c.104C>T	ENSP00000411013.2:p.Ala35Val
ENST00000482761.1:n.391C>T
NM_001256317.1:c.104C>T	NP_001243246.1:p.Ala35Val
NM_024022.2:c.104C>T	NP_076927.1:p.Ala35Val
NM_032405.1:c.104C>T	NP_115781.1:p.Ala35Val
NR_046020.1:n.1060C>T
NM_001256317.2:c.104C>T	NP_001243246.1:p.Ala35Val
NM_024022.3:c.104C>T	NP_076927.1:p.Ala35Val
NM_032405.2:c.104C>T	NP_115781.1:p.Ala35Val
NM_001256317.3:c.104C>T MANE Select	NP_001243246.1:p.Ala35Val
NM_024022.4:c.104C>T	NP_076927.1:p.Ala35Val