Canonical Allele Identifier: CA378586608
Gene: HTRA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.124268223T>A (hg19) chr10:g.122508707T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122508707T>A , CM000672.2:g.122508707T>A GRCh38
NC_000010.10:g.124268223T>A , CM000672.1:g.124268223T>A GRCh37
NC_000010.9:g.124258213T>A NCBI36
NG_011554.1:g.52183T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.1057T>A MANE Select ENSP00000357980.3:p.Phe353Ile
ENST00000648167.1:c.739T>A ENSP00000498033.1:p.Phe247Ile
ENST00000368984.7:c.1057T>A ENSP00000357980.3:p.Phe353Ile
ENST00000420892.1:c.280T>A ENSP00000412676.1:p.Phe94Ile
NM_002775.4:c.1057T>A NP_002766.1:p.Phe353Ile
NM_002775.5:c.1057T>A MANE Select NP_002766.1:p.Phe353Ile
Search 100 bp 5'
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