Canonical Allele Identifier: CA1941477187
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506699G= , CM000672.2:g.122506699G= GRCh38
NC_000010.10:g.124266215G= , CM000672.1:g.124266215G= GRCh37
NC_000010.9:g.124256205G= NCBI36
NG_011554.1:g.50175G=

Transcript Alleles

HGVS Amino-acid change
ENST00000368984.8:c.786G= MANE Select ENSP00000357980.3:p.Leu262=
ENST00000648167.1:c.468G= ENSP00000498033.1:p.Leu156=
ENST00000368984.7:c.786G= ENSP00000357980.3:p.Leu262=
ENST00000420892.1:c.9G= ENSP00000412676.1:p.Leu3=
NM_002775.4:c.786G= NP_002766.1:p.Leu262=
NM_002775.5:c.786G= MANE Select NP_002766.1:p.Leu262=