Canonical Allele Identifier: CA1941477217
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506757A= , CM000672.2:g.122506757A= GRCh38
NC_000010.10:g.124266273A= , CM000672.1:g.124266273A= GRCh37
NC_000010.9:g.124256263A= NCBI36
NG_011554.1:g.50233A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.844A= MANE Select ENSP00000357980.3:p.Ile282=
ENST00000648167.1:c.526A= ENSP00000498033.1:p.Ile176=
ENST00000368984.7:c.844A= ENSP00000357980.3:p.Ile282=
ENST00000420892.1:c.67A= ENSP00000412676.1:p.Ile23=
NM_002775.4:c.844A= NP_002766.1:p.Ile282=
NM_002775.5:c.844A= MANE Select NP_002766.1:p.Ile282=