Canonical Allele Identifier: CA1941467512
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122472329A= , CM000672.2:g.122472329A= GRCh38
NC_000010.10:g.124231845A= , CM000672.1:g.124231845A= GRCh37
NC_000010.9:g.124221835A= NCBI36
NG_011554.1:g.15805A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.472+10205A= MANE Select ENSP00000357980.3:n.472+10205A=
ENST00000648167.1:c.154+13620A= ENSP00000498033.1:n.154+13620A=
ENST00000368984.7:c.472+10205A= ENSP00000357980.3:n.472+10205A=
NM_002775.4:c.472+10205A= NP_002766.1:n.472+10205A=
NM_002775.5:c.472+10205A= MANE Select NP_002766.1:n.472+10205A=