Canonical Allele Identifier: CA2670825698
Gene: TMPRSS11A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67932022_67932023insAC , CM000666.2:g.67932022_67932023insAC GRCh38
NC_000004.11:g.68797740_68797741insAC , CM000666.1:g.68797740_68797741insAC GRCh37
NC_000004.10:g.68480335_68480336insAC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000508048.6:c.290_291insGT MANE Select ENSP00000426911.2:p.Asn97LysfsTer8
ENST00000334830.11:c.299_300insGT ENSP00000334611.7:p.Asn100LysfsTer8
ENST00000396188.3:c.290_291insGT ENSP00000379491.3:p.Asn97LysfsTer8
ENST00000508048.5:c.290_291insGT ENSP00000426911.2:p.Asn97LysfsTer8
ENST00000513536.5:c.230_231insGT ENSP00000427621.1:p.Asn77LysfsTer8
NM_001114387.1:c.290_291insGT NP_001107859.1:p.Asn97LysfsTer8
NM_182606.3:c.299_300insGT NP_872412.3:p.Asn100LysfsTer8
NM_001114387.2:c.290_291insGT MANE Select NP_001107859.1:p.Asn97LysfsTer8
NM_182606.4:c.299_300insGT NP_872412.3:p.Asn100LysfsTer8