Canonical Allele Identifier: CA1941477139
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506595C= , CM000672.2:g.122506595C= GRCh38
NC_000010.10:g.124266111C= , CM000672.1:g.124266111C= GRCh37
NC_000010.9:g.124256101C= NCBI36
NG_011554.1:g.50071C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.778-96C= MANE Select ENSP00000357980.3:n.778-96C=
ENST00000648167.1:c.460-96C= ENSP00000498033.1:n.460-96C=
ENST00000368984.7:c.778-96C= ENSP00000357980.3:n.778-96C=
NM_002775.4:c.778-96C= NP_002766.1:n.778-96C=
NM_002775.5:c.778-96C= MANE Select NP_002766.1:n.778-96C=