Canonical Allele Identifier: CA2842616629
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506892C>A , CM000672.2:g.122506892C>A GRCh38
NC_000010.10:g.124266408C>A , CM000672.1:g.124266408C>A GRCh37
NC_000010.9:g.124256398C>A NCBI36
NG_011554.1:g.50368C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.972+7C>A MANE Select ENSP00000357980.3:n.972+7C>A
ENST00000648167.1:c.654+7C>A ENSP00000498033.1:n.654+7C>A
ENST00000368984.7:c.972+7C>A ENSP00000357980.3:n.972+7C>A
ENST00000420892.1:c.195+7C>A ENSP00000412676.1:n.195+7C>A
NM_002775.4:c.972+7C>A NP_002766.1:n.972+7C>A
NM_002775.5:c.972+7C>A MANE Select NP_002766.1:n.972+7C>A