Canonical Allele Identifier: CA214389724
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs550618072
gnomAD v2: 10-124231702-C-CT
gnomAD v3: 10-122472186-C-CT
gnomAD v4: 10-122472186-C-CT
MyVariant Identifiers: chr10:g.124231703_124231704insT (hg19) chr10:g.124231702_124231703insT (hg19) chr10:g.122472187_122472188insT (hg38) chr10:g.122472186_122472187insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122472195dup , CM000672.2:g.122472195dup GRCh38
NC_000010.10:g.124231711dup , CM000672.1:g.124231711dup GRCh37
NC_000010.9:g.124221701dup NCBI36
NG_011554.1:g.15671dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.472+10071dup MANE Select ENSP00000357980.3:n.472+10071dup
ENST00000648167.1:c.154+13486dup ENSP00000498033.1:n.154+13486dup
ENST00000368984.7:c.472+10071dup ENSP00000357980.3:n.472+10071dup
NM_002775.4:c.472+10071dup NP_002766.1:n.472+10071dup
NM_002775.5:c.472+10071dup MANE Select NP_002766.1:n.472+10071dup
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Search 100 bp 3'