Canonical Allele Identifier: CA552162424
Gene: TMPRSS11A HGNC NCBI

Linked Data

dbSNP Id: rs1313211707

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67931999dup , CM000666.2:g.67931999dup GRCh38
NC_000004.11:g.68797717dup , CM000666.1:g.68797717dup GRCh37
NC_000004.10:g.68480312dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000508048.6:c.314dup MANE Select ENSP00000426911.2:p.Leu106ThrfsTer22
ENST00000334830.11:c.323dup ENSP00000334611.7:p.Leu109ThrfsTer22
ENST00000396188.3:c.314dup ENSP00000379491.3:p.Leu106ThrfsTer22
ENST00000508048.5:c.314dup ENSP00000426911.2:p.Leu106ThrfsTer22
ENST00000513536.5:c.254dup ENSP00000427621.1:p.Leu86ThrfsTer22
NM_001114387.1:c.314dup NP_001107859.1:p.Leu106ThrfsTer22
NM_182606.3:c.323dup NP_872412.3:p.Leu109ThrfsTer22
NM_001114387.2:c.314dup MANE Select NP_001107859.1:p.Leu106ThrfsTer22
NM_182606.4:c.323dup NP_872412.3:p.Leu109ThrfsTer22