Canonical Allele Identifier: CA1941478114
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122508738T= , CM000672.2:g.122508738T= GRCh38
NC_000010.10:g.124268254T= , CM000672.1:g.124268254T= GRCh37
NC_000010.9:g.124258244T= NCBI36
NG_011554.1:g.52214T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.1088T= MANE Select ENSP00000357980.3:p.Phe363=
ENST00000648167.1:c.770T= ENSP00000498033.1:p.Phe257=
ENST00000368984.7:c.1088T= ENSP00000357980.3:p.Phe363=
ENST00000420892.1:c.311T= ENSP00000412676.1:p.Phe104=
NM_002775.4:c.1088T= NP_002766.1:p.Phe363=
NM_002775.5:c.1088T= MANE Select NP_002766.1:p.Phe363=