Canonical Allele Identifier: CA2611238822
Gene: HTRA1 HGNC NCBI

Linked Data

gnomAD v4: 10-122461611-CT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461612del , CM000672.2:g.122461612del GRCh38
NC_000010.10:g.124221128del , CM000672.1:g.124221128del GRCh37
NC_000010.9:g.124211118del NCBI36
NG_011554.1:g.5088del

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.-41del MANE Select ENSP00000357980.3:n.-41del
ENST00000648167.1:c.154+2903del ENSP00000498033.1:n.154+2903del
ENST00000368984.7:c.-41del ENSP00000357980.3:n.-41del
NM_002775.4:c.-41del NP_002766.1:n.-41del
NM_002775.5:c.-41del MANE Select NP_002766.1:n.-41del
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Search 100 bp 3'