Canonical Allele Identifier: CA2842616632
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506914A>C , CM000672.2:g.122506914A>C GRCh38
NC_000010.10:g.124266430A>C , CM000672.1:g.124266430A>C GRCh37
NC_000010.9:g.124256420A>C NCBI36
NG_011554.1:g.50390A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.972+29A>C MANE Select ENSP00000357980.3:n.972+29A>C
ENST00000648167.1:c.654+29A>C ENSP00000498033.1:n.654+29A>C
ENST00000368984.7:c.972+29A>C ENSP00000357980.3:n.972+29A>C
ENST00000420892.1:c.195+29A>C ENSP00000412676.1:n.195+29A>C
NM_002775.4:c.972+29A>C NP_002766.1:n.972+29A>C
NM_002775.5:c.972+29A>C MANE Select NP_002766.1:n.972+29A>C