Canonical Allele Identifier: CA410374759

Gene: TMPRSS3

Linked Data

• dbSNP Id: rs781338726
• MyVariant Identifiers: chr21:g.43805524T>C (hg19) ; chr21:g.42385415T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42385415T>C , CM000683.2:g.42385415T>C	GRCh38
NC_000021.8:g.43805524T>C , CM000683.1:g.43805524T>C	GRCh37
NC_000021.7:g.42678593T>C	NCBI36
NG_011629.1:g.15677A>G
NG_011629.2:g.15677A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433957.7:c.566A>G	ENSP00000411013.3:p.Tyr189Cys
ENST00000644384.2:c.566A>G MANE Select	ENSP00000494414.1:p.Tyr189Cys
ENST00000652415.1:c.566A>G	ENSP00000498756.1:p.Tyr189Cys
ENST00000291532.7:c.566A>G	ENSP00000291532.3:p.Tyr189Cys
ENST00000398397.3:c.566A>G	ENSP00000381434.3:p.Tyr189Cys
ENST00000398405.5:c.560A>G	ENSP00000381442.1:p.Tyr187Cys
ENST00000433957.6:c.566A>G	ENSP00000411013.2:p.Tyr189Cys
ENST00000474596.5:n.434A>G
ENST00000482761.1:n.853A>G
NM_001256317.1:c.566A>G	NP_001243246.1:p.Tyr189Cys
NM_024022.2:c.566A>G	NP_076927.1:p.Tyr189Cys
NM_032404.2:c.185A>G	NP_115780.1:p.Tyr62Cys
NM_032405.1:c.566A>G	NP_115781.1:p.Tyr189Cys
NR_046020.1:n.1522A>G
NM_001256317.2:c.566A>G	NP_001243246.1:p.Tyr189Cys
NM_024022.3:c.566A>G	NP_076927.1:p.Tyr189Cys
NM_032405.2:c.566A>G	NP_115781.1:p.Tyr189Cys
NM_001256317.3:c.566A>G MANE Select	NP_001243246.1:p.Tyr189Cys
NM_024022.4:c.566A>G	NP_076927.1:p.Tyr189Cys
NM_032404.3:c.185A>G	NP_115780.1:p.Tyr62Cys