Canonical Allele Identifier: CA471667135
Gene: HTRA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.124268225T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122508709T>C , CM000672.2:g.122508709T>C GRCh38
NC_000010.10:g.124268225T>C , CM000672.1:g.124268225T>C GRCh37
NC_000010.9:g.124258215T>C NCBI36
NG_011554.1:g.52185T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.1059T>C MANE Select ENSP00000357980.3:p.Phe353=
ENST00000648167.1:c.741T>C ENSP00000498033.1:p.Phe247=
ENST00000368984.7:c.1059T>C ENSP00000357980.3:p.Phe353=
ENST00000420892.1:c.282T>C ENSP00000412676.1:p.Phe94=
NM_002775.4:c.1059T>C NP_002766.1:p.Phe353=
NM_002775.5:c.1059T>C MANE Select NP_002766.1:p.Phe353=