Canonical Allele Identifier: CA638062085

Gene: TMPRSS3

Linked Data

• dbSNP Id: rs1271929004
• gnomAD v2: 21-43802352-AG-A
• gnomAD v4: 21-42382243-AG-A
• MyVariant Identifiers: chr21:g.43802353del (hg19) ; chr21:g.42382244del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42382244del , CM000683.2:g.42382244del	GRCh38
NC_000021.8:g.43802353del , CM000683.1:g.43802353del	GRCh37
NC_000021.7:g.42675422del	NCBI36
NG_011629.1:g.18848del
NG_011629.2:g.18848del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433957.7:c.783-10del	ENSP00000411013.3:n.783-10del
ENST00000644384.2:c.783-10del MANE Select	ENSP00000494414.1:n.783-10del
ENST00000652415.1:c.783-10del	ENSP00000498756.1:n.783-10del
ENST00000291532.7:c.783-10del	ENSP00000291532.3:n.783-10del
ENST00000398397.3:c.783-10del	ENSP00000381434.3:n.783-10del
ENST00000398405.5:c.777-10del	ENSP00000381442.1:n.777-10del
ENST00000433957.6:c.783-10del	ENSP00000411013.2:n.783-10del
ENST00000474596.5:n.651-10del
ENST00000476848.5:n.1508del
ENST00000478680.1:n.60-10del
ENST00000482761.1:n.1070-10del
NM_001256317.1:c.783-10del	NP_001243246.1:n.783-10del
NM_024022.2:c.783-10del	NP_076927.1:n.783-10del
NM_032404.2:c.402-10del	NP_115780.1:n.402-10del
NM_032405.1:c.783-10del	NP_115781.1:n.783-10del
NR_046020.1:n.1739-10del
NM_001256317.2:c.783-10del	NP_001243246.1:n.783-10del
NM_024022.3:c.783-10del	NP_076927.1:n.783-10del
NM_032405.2:c.783-10del	NP_115781.1:n.783-10del
NM_001256317.3:c.783-10del MANE Select	NP_001243246.1:n.783-10del
NM_024022.4:c.783-10del	NP_076927.1:n.783-10del
NM_032404.3:c.402-10del	NP_115780.1:n.402-10del