Canonical Allele Identifier: CA1941477185
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506695A= , CM000672.2:g.122506695A= GRCh38
NC_000010.10:g.124266211A= , CM000672.1:g.124266211A= GRCh37
NC_000010.9:g.124256201A= NCBI36
NG_011554.1:g.50171A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.782A= MANE Select ENSP00000357980.3:p.Lys261=
ENST00000648167.1:c.464A= ENSP00000498033.1:p.Lys155=
ENST00000368984.7:c.782A= ENSP00000357980.3:p.Lys261=
ENST00000420892.1:c.5A= ENSP00000412676.1:p.Lys2=
NM_002775.4:c.782A= NP_002766.1:p.Lys261=
NM_002775.5:c.782A= MANE Select NP_002766.1:p.Lys261=