Canonical Allele Identifier: CA1941459087
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461565T= , CM000672.2:g.122461565T= GRCh38
NC_000010.10:g.124221081T= , CM000672.1:g.124221081T= GRCh37
NC_000010.9:g.124211071T= NCBI36
NG_011554.1:g.5041T=

Transcript Alleles

HGVS Amino-acid change
ENST00000368984.8:c.-88T= MANE Select ENSP00000357980.3:n.-88T=
ENST00000648167.1:c.154+2856T= ENSP00000498033.1:n.154+2856T=
ENST00000368984.7:c.-88T= ENSP00000357980.3:n.-88T=
NM_002775.4:c.-88T= NP_002766.1:n.-88T=
NM_002775.5:c.-88T= MANE Select NP_002766.1:n.-88T=