Canonical Allele Identifier: CA2722918412
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs2133911418
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122472371del , CM000672.2:g.122472371del GRCh38
NC_000010.10:g.124231887del , CM000672.1:g.124231887del GRCh37
NC_000010.9:g.124221877del NCBI36
NG_011554.1:g.15847del

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.472+10247del MANE Select ENSP00000357980.3:n.472+10247del
ENST00000648167.1:c.154+13662del ENSP00000498033.1:n.154+13662del
ENST00000368984.7:c.472+10247del ENSP00000357980.3:n.472+10247del
NM_002775.4:c.472+10247del NP_002766.1:n.472+10247del
NM_002775.5:c.472+10247del MANE Select NP_002766.1:n.472+10247del
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