Canonical Allele Identifier: CA749538388

Gene: TMPRSS3

Linked Data

• dbSNP Id: rs1460220140
• gnomAD v3: 21-42372484-AG-A
• gnomAD v4: 21-42372484-AG-A
• MyVariant Identifiers: chr21:g.43792594del (hg19) ; chr21:g.42372485del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000021.9:g.42372487del , CM000683.2:g.42372487del	GRCh38
NC_000021.8:g.43792596del , CM000683.1:g.43792596del	GRCh37
NC_000021.7:g.42665665del	NCBI36
NG_011629.1:g.28607del
NG_011629.2:g.28607del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000433957.7:c.*277del	ENSP00000411013.3:n.*277del
ENST00000644384.2:c.*277del MANE Select	ENSP00000494414.1:n.*277del
ENST00000652415.1:c.*277del	ENSP00000498756.1:n.*277del
ENST00000291532.7:c.*277del	ENSP00000291532.3:n.*277del
ENST00000398405.5:c.*277del	ENSP00000381442.1:n.*277del
ENST00000433957.6:c.*277del	ENSP00000411013.2:n.*277del
ENST00000474596.5:n.1510del
ENST00000476848.5:n.2374del
ENST00000482761.1:n.1929del
NM_001256317.1:c.*277del	NP_001243246.1:n.*277del
NM_024022.2:c.*277del	NP_076927.1:n.*277del
NM_032404.2:c.*277del	NP_115780.1:n.*277del
NR_046020.1:n.2598del
NM_001256317.2:c.*277del	NP_001243246.1:n.*277del
NM_024022.3:c.*277del	NP_076927.1:n.*277del
NM_001256317.3:c.*277del MANE Select	NP_001243246.1:n.*277del
NM_024022.4:c.*277del	NP_076927.1:n.*277del
NM_032404.3:c.*277del	NP_115780.1:n.*277del