Canonical Allele Identifier: CA1941477240
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506817C= , CM000672.2:g.122506817C= GRCh38
NC_000010.10:g.124266333C= , CM000672.1:g.124266333C= GRCh37
NC_000010.9:g.124256323C= NCBI36
NG_011554.1:g.50293C=

Transcript Alleles

HGVS Amino-acid change
ENST00000368984.8:c.904C= MANE Select ENSP00000357980.3:p.Arg302=
ENST00000648167.1:c.586C= ENSP00000498033.1:p.Arg196=
ENST00000368984.7:c.904C= ENSP00000357980.3:p.Arg302=
ENST00000420892.1:c.127C= ENSP00000412676.1:p.Arg43=
NM_002775.4:c.904C= NP_002766.1:p.Arg302=
NM_002775.5:c.904C= MANE Select NP_002766.1:p.Arg302=