Canonical Allele Identifier: CA2670825701
Gene: TMPRSS11A HGNC NCBI

Linked Data

gnomAD v4: 4-67932045-TA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67932048del , CM000666.2:g.67932048del GRCh38
NC_000004.11:g.68797766del , CM000666.1:g.68797766del GRCh37
NC_000004.10:g.68480361del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000508048.6:c.267del MANE Select ENSP00000426911.2:p.Phe89LeufsTer2
ENST00000334830.11:c.276del ENSP00000334611.7:p.Phe92LeufsTer2
ENST00000396188.3:c.267del ENSP00000379491.3:p.Phe89LeufsTer2
ENST00000508048.5:c.267del ENSP00000426911.2:p.Phe89LeufsTer2
ENST00000513536.5:c.207del ENSP00000427621.1:p.Phe69LeufsTer2
NM_001114387.1:c.267del NP_001107859.1:p.Phe89LeufsTer2
NM_182606.3:c.276del NP_872412.3:p.Phe92LeufsTer2
NM_001114387.2:c.267del MANE Select NP_001107859.1:p.Phe89LeufsTer2
NM_182606.4:c.276del NP_872412.3:p.Phe92LeufsTer2
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