Canonical Allele Identifier: CA596374928
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs1164202324
gnomAD v2: 10-124231503-TG-T
gnomAD v3: 10-122471987-TG-T
gnomAD v4: 10-122471987-TG-T
MyVariant Identifiers: chr10:g.124231504del (hg19) chr10:g.122471988del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122471988del , CM000672.2:g.122471988del GRCh38
NC_000010.10:g.124231504del , CM000672.1:g.124231504del GRCh37
NC_000010.9:g.124221494del NCBI36
NG_011554.1:g.15464del

Transcript Alleles

HGVS Amino-acid change
ENST00000368984.8:c.472+9864del MANE Select ENSP00000357980.3:n.472+9864del
ENST00000648167.1:c.154+13279del ENSP00000498033.1:n.154+13279del
ENST00000368984.7:c.472+9864del ENSP00000357980.3:n.472+9864del
NM_002775.4:c.472+9864del NP_002766.1:n.472+9864del
NM_002775.5:c.472+9864del MANE Select NP_002766.1:n.472+9864del
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Search 100 bp 3'