Canonical Allele Identifier: CA1941459693
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461858G= , CM000672.2:g.122461858G= GRCh38
NC_000010.10:g.124221374G= , CM000672.1:g.124221374G= GRCh37
NC_000010.9:g.124211364G= NCBI36
NG_011554.1:g.5334G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.206G= MANE Select ENSP00000357980.3:p.Gly69=
ENST00000648167.1:c.154+3149G= ENSP00000498033.1:n.154+3149G=
ENST00000368984.7:c.206G= ENSP00000357980.3:p.Gly69=
NM_002775.4:c.206G= NP_002766.1:p.Gly69=
NM_002775.5:c.206G= MANE Select NP_002766.1:p.Gly69=