Canonical Allele Identifier: CA1941477346
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122507065A= , CM000672.2:g.122507065A= GRCh38
NC_000010.10:g.124266581A= , CM000672.1:g.124266581A= GRCh37
NC_000010.9:g.124256571A= NCBI36
NG_011554.1:g.50541A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.972+180A= MANE Select ENSP00000357980.3:n.972+180A=
ENST00000648167.1:c.654+180A= ENSP00000498033.1:n.654+180A=
ENST00000368984.7:c.972+180A= ENSP00000357980.3:n.972+180A=
ENST00000420892.1:c.195+180A= ENSP00000412676.1:n.195+180A=
NM_002775.4:c.972+180A= NP_002766.1:n.972+180A=
NM_002775.5:c.972+180A= MANE Select NP_002766.1:n.972+180A=