Canonical Allele Identifier: CA10042449

Gene: TMPRSS3

Linked Data

• ClinVar Variation Id: 2959643
• ClinVar RCV Id: RCV003811818
• dbSNP Id: rs147785678
• ExAC: 21:43802325 T / C
• gnomAD v2: 21-43802325-T-C
• gnomAD v3: 21-42382216-T-C
• gnomAD v4: 21-42382216-T-C
• MyVariant Identifiers: chr21:g.43802325T>C (hg19) ; chr21:g.42382216T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42382216T>C , CM000683.2:g.42382216T>C	GRCh38
NC_000021.8:g.43802325T>C , CM000683.1:g.43802325T>C	GRCh37
NC_000021.7:g.42675394T>C	NCBI36
NG_011629.1:g.18876A>G
NG_011629.2:g.18876A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433957.7:c.801A>G	ENSP00000411013.3:p.Ser267=
ENST00000644384.2:c.801A>G MANE Select	ENSP00000494414.1:p.Ser267=
ENST00000652415.1:c.801A>G	ENSP00000498756.1:p.Ser267=
ENST00000291532.7:c.801A>G	ENSP00000291532.3:p.Ser267=
ENST00000398397.3:c.801A>G	ENSP00000381434.3:p.Ser267=
ENST00000398405.5:c.795A>G	ENSP00000381442.1:p.Ser265=
ENST00000433957.6:c.801A>G	ENSP00000411013.2:p.Ser267=
ENST00000474596.5:n.669A>G
ENST00000476848.5:n.1536A>G
ENST00000478680.1:n.78A>G
ENST00000482761.1:n.1088A>G
NM_001256317.1:c.801A>G	NP_001243246.1:p.Ser267=
NM_024022.2:c.801A>G	NP_076927.1:p.Ser267=
NM_032404.2:c.420A>G	NP_115780.1:p.Ser140=
NM_032405.1:c.801A>G	NP_115781.1:p.Ser267=
NR_046020.1:n.1757A>G
NM_001256317.2:c.801A>G	NP_001243246.1:p.Ser267=
NM_024022.3:c.801A>G	NP_076927.1:p.Ser267=
NM_032405.2:c.801A>G	NP_115781.1:p.Ser267=
NM_001256317.3:c.801A>G MANE Select	NP_001243246.1:p.Ser267=
NM_024022.4:c.801A>G	NP_076927.1:p.Ser267=
NM_032404.3:c.420A>G	NP_115780.1:p.Ser140=