Canonical Allele Identifier: CA1941477283
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506933A= , CM000672.2:g.122506933A= GRCh38
NC_000010.10:g.124266449A= , CM000672.1:g.124266449A= GRCh37
NC_000010.9:g.124256439A= NCBI36
NG_011554.1:g.50409A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.972+48A= MANE Select ENSP00000357980.3:n.972+48A=
ENST00000648167.1:c.654+48A= ENSP00000498033.1:n.654+48A=
ENST00000368984.7:c.972+48A= ENSP00000357980.3:n.972+48A=
ENST00000420892.1:c.195+48A= ENSP00000412676.1:n.195+48A=
NM_002775.4:c.972+48A= NP_002766.1:n.972+48A=
NM_002775.5:c.972+48A= MANE Select NP_002766.1:n.972+48A=