Canonical Allele Identifier: CA1941478103
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122508660G= , CM000672.2:g.122508660G= GRCh38
NC_000010.10:g.124268176G= , CM000672.1:g.124268176G= GRCh37
NC_000010.9:g.124258166G= NCBI36
NG_011554.1:g.52136G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.1010G= MANE Select ENSP00000357980.3:p.Gly337=
ENST00000648167.1:c.692G= ENSP00000498033.1:p.Gly231=
ENST00000368984.7:c.1010G= ENSP00000357980.3:p.Gly337=
ENST00000420892.1:c.233G= ENSP00000412676.1:p.Gly78=
NM_002775.4:c.1010G= NP_002766.1:p.Gly337=
NM_002775.5:c.1010G= MANE Select NP_002766.1:p.Gly337=