Canonical Allele Identifier: CA1941477248
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506841C= , CM000672.2:g.122506841C= GRCh38
NC_000010.10:g.124266357C= , CM000672.1:g.124266357C= GRCh37
NC_000010.9:g.124256347C= NCBI36
NG_011554.1:g.50317C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.928C= MANE Select ENSP00000357980.3:p.Arg310=
ENST00000648167.1:c.610C= ENSP00000498033.1:p.Arg204=
ENST00000368984.7:c.928C= ENSP00000357980.3:p.Arg310=
ENST00000420892.1:c.151C= ENSP00000412676.1:p.Arg51=
NM_002775.4:c.928C= NP_002766.1:p.Arg310=
NM_002775.5:c.928C= MANE Select NP_002766.1:p.Arg310=