Canonical Allele Identifier: CA378585476
Gene: HTRA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.124266271C>A (hg19) chr10:g.122506755C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506755C>A , CM000672.2:g.122506755C>A GRCh38
NC_000010.10:g.124266271C>A , CM000672.1:g.124266271C>A GRCh37
NC_000010.9:g.124256261C>A NCBI36
NG_011554.1:g.50231C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.842C>A MANE Select ENSP00000357980.3:p.Ala281Asp
ENST00000648167.1:c.524C>A ENSP00000498033.1:p.Ala175Asp
ENST00000368984.7:c.842C>A ENSP00000357980.3:p.Ala281Asp
ENST00000420892.1:c.65C>A ENSP00000412676.1:p.Ala22Asp
NM_002775.4:c.842C>A NP_002766.1:p.Ala281Asp
NM_002775.5:c.842C>A MANE Select NP_002766.1:p.Ala281Asp
Search 100 bp 5'
Search 100 bp 3'