Canonical Allele Identifier: CA2611246689
Gene: HTRA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506966del , CM000672.2:g.122506966del GRCh38
NC_000010.10:g.124266482del , CM000672.1:g.124266482del GRCh37
NC_000010.9:g.124256472del NCBI36
NG_011554.1:g.50442del

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.972+81del MANE Select ENSP00000357980.3:n.972+81del
ENST00000648167.1:c.654+81del ENSP00000498033.1:n.654+81del
ENST00000368984.7:c.972+81del ENSP00000357980.3:n.972+81del
ENST00000420892.1:c.195+81del ENSP00000412676.1:n.195+81del
NM_002775.4:c.972+81del NP_002766.1:n.972+81del
NM_002775.5:c.972+81del MANE Select NP_002766.1:n.972+81del