Canonical Allele Identifier: CA2939720
Gene: TMPRSS11A HGNC NCBI

Linked Data

dbSNP Id: rs769204666

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67932027dup , CM000666.2:g.67932027dup GRCh38
NC_000004.11:g.68797745dup , CM000666.1:g.68797745dup GRCh37
NC_000004.10:g.68480340dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000508048.6:c.290dup MANE Select ENSP00000426911.2:p.Asn97LysfsTer31
ENST00000334830.11:c.299dup ENSP00000334611.7:p.Asn100LysfsTer31
ENST00000396188.3:c.290dup ENSP00000379491.3:p.Asn97LysfsTer31
ENST00000508048.5:c.290dup ENSP00000426911.2:p.Asn97LysfsTer31
ENST00000513536.5:c.230dup ENSP00000427621.1:p.Asn77LysfsTer31
NM_001114387.1:c.290dup NP_001107859.1:p.Asn97LysfsTer31
NM_182606.3:c.299dup NP_872412.3:p.Asn100LysfsTer31
NM_001114387.2:c.290dup MANE Select NP_001107859.1:p.Asn97LysfsTer31
NM_182606.4:c.299dup NP_872412.3:p.Asn100LysfsTer31