Canonical Allele Identifier: CA410376004

Gene: TMPRSS3

Linked Data

• dbSNP Id: rs1188862235
• gnomAD v2: 21-43810128-G-A
• gnomAD v4: 21-42390019-G-A
• MyVariant Identifiers: chr21:g.43810128G>A (hg19) ; chr21:g.42390019G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42390019G>A , CM000683.2:g.42390019G>A	GRCh38
NC_000021.8:g.43810128G>A , CM000683.1:g.43810128G>A	GRCh37
NC_000021.7:g.42683197G>A	NCBI36
NG_011629.1:g.11073C>T
NG_011629.2:g.11073C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433957.7:c.113C>T	ENSP00000411013.3:p.Ala38Val
ENST00000644384.2:c.113C>T MANE Select	ENSP00000494414.1:p.Ala38Val
ENST00000652415.1:c.113C>T	ENSP00000498756.1:p.Ala38Val
ENST00000291532.7:c.113C>T	ENSP00000291532.3:p.Ala38Val
ENST00000398397.3:c.113C>T	ENSP00000381434.3:p.Ala38Val
ENST00000398405.5:c.107C>T	ENSP00000381442.1:p.Ala36Val
ENST00000433957.6:c.113C>T	ENSP00000411013.2:p.Ala38Val
ENST00000482761.1:n.400C>T
NM_001256317.1:c.113C>T	NP_001243246.1:p.Ala38Val
NM_024022.2:c.113C>T	NP_076927.1:p.Ala38Val
NM_032405.1:c.113C>T	NP_115781.1:p.Ala38Val
NR_046020.1:n.1069C>T
NM_001256317.2:c.113C>T	NP_001243246.1:p.Ala38Val
NM_024022.3:c.113C>T	NP_076927.1:p.Ala38Val
NM_032405.2:c.113C>T	NP_115781.1:p.Ala38Val
NM_001256317.3:c.113C>T MANE Select	NP_001243246.1:p.Ala38Val
NM_024022.4:c.113C>T	NP_076927.1:p.Ala38Val