Canonical Allele Identifier: CA1941477260
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506873C= , CM000672.2:g.122506873C= GRCh38
NC_000010.10:g.124266389C= , CM000672.1:g.124266389C= GRCh37
NC_000010.9:g.124256379C= NCBI36
NG_011554.1:g.50349C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.960C= MANE Select ENSP00000357980.3:p.Asp320=
ENST00000648167.1:c.642C= ENSP00000498033.1:p.Asp214=
ENST00000368984.7:c.960C= ENSP00000357980.3:p.Asp320=
ENST00000420892.1:c.183C= ENSP00000412676.1:p.Asp61=
NM_002775.4:c.960C= NP_002766.1:p.Asp320=
NM_002775.5:c.960C= MANE Select NP_002766.1:p.Asp320=