Canonical Allele Identifier: CA1941467505
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122472316_122472319delinsAAAG , CM000672.2:g.122472316_122472319delinsAAAG GRCh38
NC_000010.10:g.124231832_124231835delinsAAAG , CM000672.1:g.124231832_124231835delinsAAAG GRCh37
NC_000010.9:g.124221822_124221825delinsAAAG NCBI36
NG_011554.1:g.15792_15795delinsAAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.472+10192_472+10195delinsAAAG MANE Select ENSP00000357980.3:n.472+10192_472+10195delinsAAAG
ENST00000648167.1:c.154+13607_154+13610delinsAAAG ENSP00000498033.1:n.154+13607_154+13610delinsAAAG
ENST00000368984.7:c.472+10192_472+10195delinsAAAG ENSP00000357980.3:n.472+10192_472+10195delinsAAAG
NM_002775.4:c.472+10192_472+10195delinsAAAG NP_002766.1:n.472+10192_472+10195delinsAAAG
NM_002775.5:c.472+10192_472+10195delinsAAAG MANE Select NP_002766.1:n.472+10192_472+10195delinsAAAG