Canonical Allele Identifier: CA1941477189
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506701C= , CM000672.2:g.122506701C= GRCh38
NC_000010.10:g.124266217C= , CM000672.1:g.124266217C= GRCh37
NC_000010.9:g.124256207C= NCBI36
NG_011554.1:g.50177C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.788C= MANE Select ENSP00000357980.3:p.Pro263=
ENST00000648167.1:c.470C= ENSP00000498033.1:p.Pro157=
ENST00000368984.7:c.788C= ENSP00000357980.3:p.Pro263=
ENST00000420892.1:c.11C= ENSP00000412676.1:p.Pro4=
NM_002775.4:c.788C= NP_002766.1:p.Pro263=
NM_002775.5:c.788C= MANE Select NP_002766.1:p.Pro263=