Canonical Allele Identifier: CA1941477267
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506888G= , CM000672.2:g.122506888G= GRCh38
NC_000010.10:g.124266404G= , CM000672.1:g.124266404G= GRCh37
NC_000010.9:g.124256394G= NCBI36
NG_011554.1:g.50364G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.972+3G= MANE Select ENSP00000357980.3:n.972+3G=
ENST00000648167.1:c.654+3G= ENSP00000498033.1:n.654+3G=
ENST00000368984.7:c.972+3G= ENSP00000357980.3:n.972+3G=
ENST00000420892.1:c.195+3G= ENSP00000412676.1:n.195+3G=
NM_002775.4:c.972+3G= NP_002766.1:n.972+3G=
NM_002775.5:c.972+3G= MANE Select NP_002766.1:n.972+3G=