Canonical Allele Identifier: CA797724075

Gene: TMPRSS11A

Linked Data

• dbSNP Id: rs1227357817
• gnomAD v3: 4-67932092-A-C
• gnomAD v4: 4-67932092-A-C
• MyVariant Identifiers: chr4:g.68797810A>C (hg19) ; chr4:g.67932092A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.67932092A>C , CM000666.2:g.67932092A>C	GRCh38
NC_000004.11:g.68797810A>C , CM000666.1:g.68797810A>C	GRCh37
NC_000004.10:g.68480405A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508048.6:c.253-32T>G MANE Select	ENSP00000426911.2:n.253-32T>G
ENST00000334830.11:c.262-32T>G	ENSP00000334611.7:n.262-32T>G
ENST00000396188.3:c.253-32T>G	ENSP00000379491.3:n.253-32T>G
ENST00000508048.5:c.253-32T>G	ENSP00000426911.2:n.253-32T>G
ENST00000513536.5:c.193-32T>G	ENSP00000427621.1:n.193-32T>G
NM_001114387.1:c.253-32T>G	NP_001107859.1:n.253-32T>G
NM_182606.3:c.262-32T>G	NP_872412.3:n.262-32T>G
NM_001114387.2:c.253-32T>G MANE Select	NP_001107859.1:n.253-32T>G
NM_182606.4:c.262-32T>G	NP_872412.3:n.262-32T>G