Canonical Allele Identifier: CA2670825765
Gene: TMPRSS11A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67932151_67932181del , CM000666.2:g.67932151_67932181del GRCh38
NC_000004.11:g.68797869_68797899del , CM000666.1:g.68797869_68797899del GRCh37
NC_000004.10:g.68480464_68480494del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000508048.6:c.253-116_253-86del MANE Select ENSP00000426911.2:n.253-116_253-86del
ENST00000334830.11:c.262-116_262-86del ENSP00000334611.7:n.262-116_262-86del
ENST00000396188.3:c.253-116_253-86del ENSP00000379491.3:n.253-116_253-86del
ENST00000508048.5:c.253-116_253-86del ENSP00000426911.2:n.253-116_253-86del
ENST00000513536.5:c.193-116_193-86del ENSP00000427621.1:n.193-116_193-86del
NM_001114387.1:c.253-116_253-86del NP_001107859.1:n.253-116_253-86del
NM_182606.3:c.262-116_262-86del NP_872412.3:n.262-116_262-86del
NM_001114387.2:c.253-116_253-86del MANE Select NP_001107859.1:n.253-116_253-86del
NM_182606.4:c.262-116_262-86del NP_872412.3:n.262-116_262-86del