Canonical Allele Identifier: CA1465503665
Gene: TMPRSS11A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67932022A= , CM000666.2:g.67932022A= GRCh38
NC_000004.11:g.68797740A= , CM000666.1:g.68797740A= GRCh37
NC_000004.10:g.68480335A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000508048.6:c.291T= MANE Select ENSP00000426911.2:p.Asn97=
ENST00000334830.11:c.300T= ENSP00000334611.7:p.Asn100=
ENST00000396188.3:c.291T= ENSP00000379491.3:p.Asn97=
ENST00000508048.5:c.291T= ENSP00000426911.2:p.Asn97=
ENST00000513536.5:c.231T= ENSP00000427621.1:p.Asn77=
NM_001114387.1:c.291T= NP_001107859.1:p.Asn97=
NM_182606.3:c.300T= NP_872412.3:p.Asn100=
NM_001114387.2:c.291T= MANE Select NP_001107859.1:p.Asn97=
NM_182606.4:c.300T= NP_872412.3:p.Asn100=