Canonical Allele Identifier: CA1941477289
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506938G= , CM000672.2:g.122506938G= GRCh38
NC_000010.10:g.124266454G= , CM000672.1:g.124266454G= GRCh37
NC_000010.9:g.124256444G= NCBI36
NG_011554.1:g.50414G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.972+53G= MANE Select ENSP00000357980.3:n.972+53G=
ENST00000648167.1:c.654+53G= ENSP00000498033.1:n.654+53G=
ENST00000368984.7:c.972+53G= ENSP00000357980.3:n.972+53G=
ENST00000420892.1:c.195+53G= ENSP00000412676.1:n.195+53G=
NM_002775.4:c.972+53G= NP_002766.1:n.972+53G=
NM_002775.5:c.972+53G= MANE Select NP_002766.1:n.972+53G=