Canonical Allele Identifier: CA2670825695
Gene: TMPRSS11A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67931983del , CM000666.2:g.67931983del GRCh38
NC_000004.11:g.68797701del , CM000666.1:g.68797701del GRCh37
NC_000004.10:g.68480296del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000508048.6:c.320+12del MANE Select ENSP00000426911.2:n.320+12del
ENST00000334830.11:c.329+12del ENSP00000334611.7:n.329+12del
ENST00000396188.3:c.320+12del ENSP00000379491.3:n.320+12del
ENST00000508048.5:c.320+12del ENSP00000426911.2:n.320+12del
ENST00000513536.5:c.260+12del ENSP00000427621.1:n.260+12del
NM_001114387.1:c.320+12del NP_001107859.1:n.320+12del
NM_182606.3:c.329+12del NP_872412.3:n.329+12del
NM_001114387.2:c.320+12del MANE Select NP_001107859.1:n.320+12del
NM_182606.4:c.329+12del NP_872412.3:n.329+12del