Canonical Allele Identifier: CA357064546
Gene: TMPRSS11A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67932046A>T , CM000666.2:g.67932046A>T GRCh38
NC_000004.11:g.68797764A>T , CM000666.1:g.68797764A>T GRCh37
NC_000004.10:g.68480359A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000508048.6:c.267T>A MANE Select ENSP00000426911.2:p.Phe89Leu
ENST00000334830.11:c.276T>A ENSP00000334611.7:p.Phe92Leu
ENST00000396188.3:c.267T>A ENSP00000379491.3:p.Phe89Leu
ENST00000508048.5:c.267T>A ENSP00000426911.2:p.Phe89Leu
ENST00000513536.5:c.207T>A ENSP00000427621.1:p.Phe69Leu
NM_001114387.1:c.267T>A NP_001107859.1:p.Phe89Leu
NM_182606.3:c.276T>A NP_872412.3:p.Phe92Leu
NM_001114387.2:c.267T>A MANE Select NP_001107859.1:p.Phe89Leu
NM_182606.4:c.276T>A NP_872412.3:p.Phe92Leu