Canonical Allele Identifier: CA1941459329
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461697G= , CM000672.2:g.122461697G= GRCh38
NC_000010.10:g.124221213G= , CM000672.1:g.124221213G= GRCh37
NC_000010.9:g.124211203G= NCBI36
NG_011554.1:g.5173G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.45G= MANE Select ENSP00000357980.3:p.Leu15=
ENST00000648167.1:c.154+2988G= ENSP00000498033.1:n.154+2988G=
ENST00000368984.7:c.45G= ENSP00000357980.3:p.Leu15=
NM_002775.4:c.45G= NP_002766.1:p.Leu15=
NM_002775.5:c.45G= MANE Select NP_002766.1:p.Leu15=