Canonical Allele Identifier: CA471667108
Gene: HTRA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.124268192T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122508676T>A , CM000672.2:g.122508676T>A GRCh38
NC_000010.10:g.124268192T>A , CM000672.1:g.124268192T>A GRCh37
NC_000010.9:g.124258182T>A NCBI36
NG_011554.1:g.52152T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.1026T>A MANE Select ENSP00000357980.3:p.Ile342=
ENST00000648167.1:c.708T>A ENSP00000498033.1:p.Ile236=
ENST00000368984.7:c.1026T>A ENSP00000357980.3:p.Ile342=
ENST00000420892.1:c.249T>A ENSP00000412676.1:p.Ile83=
NM_002775.4:c.1026T>A NP_002766.1:p.Ile342=
NM_002775.5:c.1026T>A MANE Select NP_002766.1:p.Ile342=