Canonical Allele Identifier: CA1465503607
Gene: TMPRSS11A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67931988C= , CM000666.2:g.67931988C= GRCh38
NC_000004.11:g.68797706C= , CM000666.1:g.68797706C= GRCh37
NC_000004.10:g.68480301C= NCBI36

Transcript Alleles

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