Canonical Allele Identifier: CA1941459804
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461928C= , CM000672.2:g.122461928C= GRCh38
NC_000010.10:g.124221444C= , CM000672.1:g.124221444C= GRCh37
NC_000010.9:g.124211434C= NCBI36
NG_011554.1:g.5404C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.276C= MANE Select ENSP00000357980.3:p.Pro92=
ENST00000648167.1:c.154+3219C= ENSP00000498033.1:n.154+3219C=
ENST00000368984.7:c.276C= ENSP00000357980.3:p.Pro92=
NM_002775.4:c.276C= NP_002766.1:p.Pro92=
NM_002775.5:c.276C= MANE Select NP_002766.1:p.Pro92=