Canonical Allele Identifier: CA357064381
Gene: TMPRSS11A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67931996A>C , CM000666.2:g.67931996A>C GRCh38
NC_000004.11:g.68797714A>C , CM000666.1:g.68797714A>C GRCh37
NC_000004.10:g.68480309A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000508048.6:c.317T>G MANE Select ENSP00000426911.2:p.Leu106Arg
ENST00000334830.11:c.326T>G ENSP00000334611.7:p.Leu109Arg
ENST00000396188.3:c.317T>G ENSP00000379491.3:p.Leu106Arg
ENST00000508048.5:c.317T>G ENSP00000426911.2:p.Leu106Arg
ENST00000513536.5:c.257T>G ENSP00000427621.1:p.Leu86Arg
NM_001114387.1:c.317T>G NP_001107859.1:p.Leu106Arg
NM_182606.3:c.326T>G NP_872412.3:p.Leu109Arg
NM_001114387.2:c.317T>G MANE Select NP_001107859.1:p.Leu106Arg
NM_182606.4:c.326T>G NP_872412.3:p.Leu109Arg