Canonical Allele Identifier: CA357064378
Gene: TMPRSS11A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67931994T>A , CM000666.2:g.67931994T>A GRCh38
NC_000004.11:g.68797712T>A , CM000666.1:g.68797712T>A GRCh37
NC_000004.10:g.68480307T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000508048.6:c.319A>T MANE Select ENSP00000426911.2:p.Thr107Ser
ENST00000334830.11:c.328A>T ENSP00000334611.7:p.Thr110Ser
ENST00000396188.3:c.319A>T ENSP00000379491.3:p.Thr107Ser
ENST00000508048.5:c.319A>T ENSP00000426911.2:p.Thr107Ser
ENST00000513536.5:c.259A>T ENSP00000427621.1:p.Thr87Ser
NM_001114387.1:c.319A>T NP_001107859.1:p.Thr107Ser
NM_182606.3:c.328A>T NP_872412.3:p.Thr110Ser
NM_001114387.2:c.319A>T MANE Select NP_001107859.1:p.Thr107Ser
NM_182606.4:c.328A>T NP_872412.3:p.Thr110Ser