Canonical Allele Identifier: CA1941459187
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461624C= , CM000672.2:g.122461624C= GRCh38
NC_000010.10:g.124221140C= , CM000672.1:g.124221140C= GRCh37
NC_000010.9:g.124211130C= NCBI36
NG_011554.1:g.5100C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.-29C= MANE Select ENSP00000357980.3:n.-29C=
ENST00000648167.1:c.154+2915C= ENSP00000498033.1:n.154+2915C=
ENST00000368984.7:c.-29C= ENSP00000357980.3:n.-29C=
NM_002775.4:c.-29C= NP_002766.1:n.-29C=
NM_002775.5:c.-29C= MANE Select NP_002766.1:n.-29C=