Canonical Allele Identifier: CA214412517
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs35887825

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122508597dup , CM000672.2:g.122508597dup GRCh38
NC_000010.10:g.124268113dup , CM000672.1:g.124268113dup GRCh37
NC_000010.9:g.124258103dup NCBI36
NG_011554.1:g.52073dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.1006-59dup MANE Select ENSP00000357980.3:n.1006-59dup
ENST00000648167.1:c.688-59dup ENSP00000498033.1:n.688-59dup
ENST00000368984.7:c.1006-59dup ENSP00000357980.3:n.1006-59dup
ENST00000420892.1:c.229-59dup ENSP00000412676.1:n.229-59dup
NM_002775.4:c.1006-59dup NP_002766.1:n.1006-59dup
NM_002775.5:c.1006-59dup MANE Select NP_002766.1:n.1006-59dup