Canonical Allele Identifier: CA1941459964
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122462054C= , CM000672.2:g.122462054C= GRCh38
NC_000010.10:g.124221570C= , CM000672.1:g.124221570C= GRCh37
NC_000010.9:g.124211560C= NCBI36
NG_011554.1:g.5530C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.402C= MANE Select ENSP00000357980.3:p.Ala134=
ENST00000648167.1:c.154+3345C= ENSP00000498033.1:n.154+3345C=
ENST00000368984.7:c.402C= ENSP00000357980.3:p.Ala134=
NM_002775.4:c.402C= NP_002766.1:p.Ala134=
NM_002775.5:c.402C= MANE Select NP_002766.1:p.Ala134=