Canonical Allele Identifier: CA749515128

Gene: TMPRSS3

Linked Data

• ClinVar Variation Id: 2779070
• ClinVar RCV Id: RCV003663377
• dbSNP Id: rs1267394254
• MyVariant Identifiers: chr21:g.43808654G>C (hg19) ; chr21:g.42388545G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42388545G>C , CM000683.2:g.42388545G>C	GRCh38
NC_000021.8:g.43808654G>C , CM000683.1:g.43808654G>C	GRCh37
NC_000021.7:g.42681723G>C	NCBI36
NG_011629.1:g.12547C>G
NG_011629.2:g.12547C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000433957.7:c.323-19C>G	ENSP00000411013.3:n.323-19C>G
ENST00000644384.2:c.323-19C>G MANE Select	ENSP00000494414.1:n.323-19C>G
ENST00000652415.1:c.323-19C>G	ENSP00000498756.1:n.323-19C>G
ENST00000291532.7:c.323-19C>G	ENSP00000291532.3:n.323-19C>G
ENST00000398397.3:c.323-19C>G	ENSP00000381434.3:n.323-19C>G
ENST00000398405.5:c.317-19C>G	ENSP00000381442.1:n.317-19C>G
ENST00000433957.6:c.323-19C>G	ENSP00000411013.2:n.323-19C>G
ENST00000474596.5:n.191-19C>G
ENST00000482761.1:n.610-19C>G
NM_001256317.1:c.323-19C>G	NP_001243246.1:n.323-19C>G
NM_024022.2:c.323-19C>G	NP_076927.1:n.323-19C>G
NM_032404.2:c.-59-19C>G	NP_115780.1:n.-59-19C>G
NM_032405.1:c.323-19C>G	NP_115781.1:n.323-19C>G
NR_046020.1:n.1279-19C>G
NM_001256317.2:c.323-19C>G	NP_001243246.1:n.323-19C>G
NM_024022.3:c.323-19C>G	NP_076927.1:n.323-19C>G
NM_032405.2:c.323-19C>G	NP_115781.1:n.323-19C>G
NM_001256317.3:c.323-19C>G MANE Select	NP_001243246.1:n.323-19C>G
NM_024022.4:c.323-19C>G	NP_076927.1:n.323-19C>G
NM_032404.3:c.-59-19C>G	NP_115780.1:n.-59-19C>G