Canonical Allele Identifier: CA410372217

Gene: TMPRSS3

Linked Data

• MyVariant Identifiers: chr21:g.43802119A>G (hg19) ; chr21:g.42382010A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42382010A>G , CM000683.2:g.42382010A>G	GRCh38
NC_000021.8:g.43802119A>G , CM000683.1:g.43802119A>G	GRCh37
NC_000021.7:g.42675188A>G	NCBI36
NG_011629.1:g.19082T>C
NG_011629.2:g.19082T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433957.7:c.952+55T>C	ENSP00000411013.3:n.952+55T>C
ENST00000644384.2:c.952+55T>C MANE Select	ENSP00000494414.1:n.952+55T>C
ENST00000652415.1:c.952+55T>C	ENSP00000498756.1:n.952+55T>C
ENST00000291532.7:c.952+55T>C	ENSP00000291532.3:n.952+55T>C
ENST00000398397.3:c.1007T>C	ENSP00000381434.3:p.Leu336Ser
ENST00000398405.5:c.946+55T>C	ENSP00000381442.1:n.946+55T>C
ENST00000433957.6:c.952+55T>C	ENSP00000411013.2:n.952+55T>C
ENST00000474596.5:n.820+55T>C
ENST00000476848.5:n.1687+55T>C
ENST00000478680.1:n.284T>C
ENST00000482761.1:n.1239+55T>C
NM_001256317.1:c.952+55T>C	NP_001243246.1:n.952+55T>C
NM_024022.2:c.952+55T>C	NP_076927.1:n.952+55T>C
NM_032404.2:c.571+55T>C	NP_115780.1:n.571+55T>C
NM_032405.1:c.1007T>C	NP_115781.1:p.Leu336Ser
NR_046020.1:n.1908+55T>C
NM_001256317.2:c.952+55T>C	NP_001243246.1:n.952+55T>C
NM_024022.3:c.952+55T>C	NP_076927.1:n.952+55T>C
NM_032405.2:c.1007T>C	NP_115781.1:p.Leu336Ser
NM_001256317.3:c.952+55T>C MANE Select	NP_001243246.1:n.952+55T>C
NM_024022.4:c.952+55T>C	NP_076927.1:n.952+55T>C
NM_032404.3:c.571+55T>C	NP_115780.1:n.571+55T>C