Canonical Allele Identifier: CA1941459272
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461677C= , CM000672.2:g.122461677C= GRCh38
NC_000010.10:g.124221193C= , CM000672.1:g.124221193C= GRCh37
NC_000010.9:g.124211183C= NCBI36
NG_011554.1:g.5153C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.25C= MANE Select ENSP00000357980.3:p.Leu9=
ENST00000648167.1:c.154+2968C= ENSP00000498033.1:n.154+2968C=
ENST00000368984.7:c.25C= ENSP00000357980.3:p.Leu9=
NM_002775.4:c.25C= NP_002766.1:p.Leu9=
NM_002775.5:c.25C= MANE Select NP_002766.1:p.Leu9=