Canonical Allele Identifier: CA1941467522
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs2097486489
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122472342del , CM000672.2:g.122472342del GRCh38
NC_000010.10:g.124231858del , CM000672.1:g.124231858del GRCh37
NC_000010.9:g.124221848del NCBI36
NG_011554.1:g.15818del

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.472+10218del MANE Select ENSP00000357980.3:n.472+10218del
ENST00000648167.1:c.154+13633del ENSP00000498033.1:n.154+13633del
ENST00000368984.7:c.472+10218del ENSP00000357980.3:n.472+10218del
NM_002775.4:c.472+10218del NP_002766.1:n.472+10218del
NM_002775.5:c.472+10218del MANE Select NP_002766.1:n.472+10218del
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