Canonical Allele Identifier: CA749547970

Gene: TMPRSS3

Linked Data

• dbSNP Id: rs1314718121
• gnomAD v3: 21-42385398-T-C
• gnomAD v4: 21-42385398-T-C
• MyVariant Identifiers: chr21:g.43805507T>C (hg19) ; chr21:g.42385398T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42385398T>C , CM000683.2:g.42385398T>C	GRCh38
NC_000021.8:g.43805507T>C , CM000683.1:g.43805507T>C	GRCh37
NC_000021.7:g.42678576T>C	NCBI36
NG_011629.1:g.15694A>G
NG_011629.2:g.15694A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000433957.7:c.572+11A>G	ENSP00000411013.3:n.572+11A>G
ENST00000644384.2:c.572+11A>G MANE Select	ENSP00000494414.1:n.572+11A>G
ENST00000652415.1:c.572+11A>G	ENSP00000498756.1:n.572+11A>G
ENST00000291532.7:c.572+11A>G	ENSP00000291532.3:n.572+11A>G
ENST00000398397.3:c.572+11A>G	ENSP00000381434.3:n.572+11A>G
ENST00000398405.5:c.566+11A>G	ENSP00000381442.1:n.566+11A>G
ENST00000433957.6:c.572+11A>G	ENSP00000411013.2:n.572+11A>G
ENST00000474596.5:n.440+11A>G
ENST00000482761.1:n.859+11A>G
NM_001256317.1:c.572+11A>G	NP_001243246.1:n.572+11A>G
NM_024022.2:c.572+11A>G	NP_076927.1:n.572+11A>G
NM_032404.2:c.191+11A>G	NP_115780.1:n.191+11A>G
NM_032405.1:c.572+11A>G	NP_115781.1:n.572+11A>G
NR_046020.1:n.1528+11A>G
NM_001256317.2:c.572+11A>G	NP_001243246.1:n.572+11A>G
NM_024022.3:c.572+11A>G	NP_076927.1:n.572+11A>G
NM_032405.2:c.572+11A>G	NP_115781.1:n.572+11A>G
NM_001256317.3:c.572+11A>G MANE Select	NP_001243246.1:n.572+11A>G
NM_024022.4:c.572+11A>G	NP_076927.1:n.572+11A>G
NM_032404.3:c.191+11A>G	NP_115780.1:n.191+11A>G