Canonical Allele Identifier: CA214389855
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs900990758
gnomAD v2: 10-124231878-TTTATTACTA-T
gnomAD v3: 10-122472362-TTTATTACTA-T
gnomAD v4: 10-122472362-TTTATTACTA-T
MyVariant Identifiers: chr10:g.124231882_124231890del (hg19) chr10:g.124231879_124231887del (hg19) chr10:g.122472366_122472374del (hg38) chr10:g.122472363_122472371del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122472369_122472377del , CM000672.2:g.122472369_122472377del GRCh38
NC_000010.10:g.124231885_124231893del , CM000672.1:g.124231885_124231893del GRCh37
NC_000010.9:g.124221875_124221883del NCBI36
NG_011554.1:g.15845_15853del

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.472+10245_472+10253del MANE Select ENSP00000357980.3:n.472+10245_472+10253del
ENST00000648167.1:c.154+13660_154+13668del ENSP00000498033.1:n.154+13660_154+13668del
ENST00000368984.7:c.472+10245_472+10253del ENSP00000357980.3:n.472+10245_472+10253del
NM_002775.4:c.472+10245_472+10253del NP_002766.1:n.472+10245_472+10253del
NM_002775.5:c.472+10245_472+10253del MANE Select NP_002766.1:n.472+10245_472+10253del
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