Canonical Allele Identifier: CA596374953
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs1446256924
gnomAD v2: 10-124231891-T-TTAC
gnomAD v3: 10-122472375-T-TTAC
gnomAD v4: 10-122472375-T-TTAC
MyVariant Identifiers: chr10:g.124231891_124231892insTAC (hg19) chr10:g.122472375_122472376insTAC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122472377_122472378insCTA , CM000672.2:g.122472377_122472378insCTA GRCh38
NC_000010.10:g.124231893_124231894insCTA , CM000672.1:g.124231893_124231894insCTA GRCh37
NC_000010.9:g.124221883_124221884insCTA NCBI36
NG_011554.1:g.15853_15854insCTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.472+10253_472+10254insCTA MANE Select ENSP00000357980.3:n.472+10253_472+10254insCTA
ENST00000648167.1:c.154+13668_154+13669insCTA ENSP00000498033.1:n.154+13668_154+13669insCTA
ENST00000368984.7:c.472+10253_472+10254insCTA ENSP00000357980.3:n.472+10253_472+10254insCTA
NM_002775.4:c.472+10253_472+10254insCTA NP_002766.1:n.472+10253_472+10254insCTA
NM_002775.5:c.472+10253_472+10254insCTA MANE Select NP_002766.1:n.472+10253_472+10254insCTA
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