Canonical Allele Identifier: CA1465503671
Gene: TMPRSS11A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67932028C= , CM000666.2:g.67932028C= GRCh38
NC_000004.11:g.68797746C= , CM000666.1:g.68797746C= GRCh37
NC_000004.10:g.68480341C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000508048.6:c.285G= MANE Select ENSP00000426911.2:p.Lys95=
ENST00000334830.11:c.294G= ENSP00000334611.7:p.Lys98=
ENST00000396188.3:c.285G= ENSP00000379491.3:p.Lys95=
ENST00000508048.5:c.285G= ENSP00000426911.2:p.Lys95=
ENST00000513536.5:c.225G= ENSP00000427621.1:p.Lys75=
NM_001114387.1:c.285G= NP_001107859.1:p.Lys95=
NM_182606.3:c.294G= NP_872412.3:p.Lys98=
NM_001114387.2:c.285G= MANE Select NP_001107859.1:p.Lys95=
NM_182606.4:c.294G= NP_872412.3:p.Lys98=