Canonical Allele Identifier: CA2654681362

Gene: TMPRSS3

Linked Data

• gnomAD v4: 21-42389894-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42389894T>C , CM000683.2:g.42389894T>C	GRCh38
NC_000021.8:g.43810003T>C , CM000683.1:g.43810003T>C	GRCh37
NC_000021.7:g.42683072T>C	NCBI36
NG_011629.1:g.11198A>G
NG_011629.2:g.11198A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433957.7:c.205+33A>G	ENSP00000411013.3:n.205+33A>G
ENST00000644384.2:c.205+33A>G MANE Select	ENSP00000494414.1:n.205+33A>G
ENST00000652415.1:c.205+33A>G	ENSP00000498756.1:n.205+33A>G
ENST00000291532.7:c.205+33A>G	ENSP00000291532.3:n.205+33A>G
ENST00000398397.3:c.205+33A>G	ENSP00000381434.3:n.205+33A>G
ENST00000398405.5:c.199+33A>G	ENSP00000381442.1:n.199+33A>G
ENST00000433957.6:c.205+33A>G	ENSP00000411013.2:n.205+33A>G
ENST00000482761.1:n.492+33A>G
NM_001256317.1:c.205+33A>G	NP_001243246.1:n.205+33A>G
NM_024022.2:c.205+33A>G	NP_076927.1:n.205+33A>G
NM_032405.1:c.205+33A>G	NP_115781.1:n.205+33A>G
NR_046020.1:n.1161+33A>G
NM_001256317.2:c.205+33A>G	NP_001243246.1:n.205+33A>G
NM_024022.3:c.205+33A>G	NP_076927.1:n.205+33A>G
NM_032405.2:c.205+33A>G	NP_115781.1:n.205+33A>G
NM_001256317.3:c.205+33A>G MANE Select	NP_001243246.1:n.205+33A>G
NM_024022.4:c.205+33A>G	NP_076927.1:n.205+33A>G