Canonical Allele Identifier: CA1941477271
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506897_122506898delinsTC , CM000672.2:g.122506897_122506898delinsTC GRCh38
NC_000010.10:g.124266413_124266414delinsTC , CM000672.1:g.124266413_124266414delinsTC GRCh37
NC_000010.9:g.124256403_124256404delinsTC NCBI36
NG_011554.1:g.50373_50374delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.972+12_972+13delinsTC MANE Select ENSP00000357980.3:n.972+12_972+13delinsTC
ENST00000648167.1:c.654+12_654+13delinsTC ENSP00000498033.1:n.654+12_654+13delinsTC
ENST00000368984.7:c.972+12_972+13delinsTC ENSP00000357980.3:n.972+12_972+13delinsTC
ENST00000420892.1:c.195+12_195+13delinsTC ENSP00000412676.1:n.195+12_195+13delinsTC
NM_002775.4:c.972+12_972+13delinsTC NP_002766.1:n.972+12_972+13delinsTC
NM_002775.5:c.972+12_972+13delinsTC MANE Select NP_002766.1:n.972+12_972+13delinsTC