Canonical Allele Identifier: CA1941477220
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506760G= , CM000672.2:g.122506760G= GRCh38
NC_000010.10:g.124266276G= , CM000672.1:g.124266276G= GRCh37
NC_000010.9:g.124256266G= NCBI36
NG_011554.1:g.50236G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.847G= MANE Select ENSP00000357980.3:p.Gly283=
ENST00000648167.1:c.529G= ENSP00000498033.1:p.Gly177=
ENST00000368984.7:c.847G= ENSP00000357980.3:p.Gly283=
ENST00000420892.1:c.70G= ENSP00000412676.1:p.Gly24=
NM_002775.4:c.847G= NP_002766.1:p.Gly283=
NM_002775.5:c.847G= MANE Select NP_002766.1:p.Gly283=