Canonical Allele Identifier: CA1941467412
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122472129_122472131delinsTGG , CM000672.2:g.122472129_122472131delinsTGG GRCh38
NC_000010.10:g.124231645_124231647delinsTGG , CM000672.1:g.124231645_124231647delinsTGG GRCh37
NC_000010.9:g.124221635_124221637delinsTGG NCBI36
NG_011554.1:g.15605_15607delinsTGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.472+10005_472+10007delinsTGG MANE Select ENSP00000357980.3:n.472+10005_472+10007delinsTGG
ENST00000648167.1:c.154+13420_154+13422delinsTGG ENSP00000498033.1:n.154+13420_154+13422delinsTGG
ENST00000368984.7:c.472+10005_472+10007delinsTGG ENSP00000357980.3:n.472+10005_472+10007delinsTGG
NM_002775.4:c.472+10005_472+10007delinsTGG NP_002766.1:n.472+10005_472+10007delinsTGG
NM_002775.5:c.472+10005_472+10007delinsTGG MANE Select NP_002766.1:n.472+10005_472+10007delinsTGG