Canonical Allele Identifier: CA1465503555
Gene: TMPRSS11A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67931942G= , CM000666.2:g.67931942G= GRCh38
NC_000004.11:g.68797660G= , CM000666.1:g.68797660G= GRCh37
NC_000004.10:g.68480255G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000508048.6:c.320+51C= MANE Select ENSP00000426911.2:n.320+51C=
ENST00000334830.11:c.329+51C= ENSP00000334611.7:n.329+51C=
ENST00000396188.3:c.320+51C= ENSP00000379491.3:n.320+51C=
ENST00000508048.5:c.320+51C= ENSP00000426911.2:n.320+51C=
ENST00000513536.5:c.260+51C= ENSP00000427621.1:n.260+51C=
NM_001114387.1:c.320+51C= NP_001107859.1:n.320+51C=
NM_182606.3:c.329+51C= NP_872412.3:n.329+51C=
NM_001114387.2:c.320+51C= MANE Select NP_001107859.1:n.320+51C=
NM_182606.4:c.329+51C= NP_872412.3:n.329+51C=
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