Canonical Allele Identifier: CA1941478047
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122508525_122508526delinsTC , CM000672.2:g.122508525_122508526delinsTC GRCh38
NC_000010.10:g.124268041_124268042delinsTC , CM000672.1:g.124268041_124268042delinsTC GRCh37
NC_000010.9:g.124258031_124258032delinsTC NCBI36
NG_011554.1:g.52001_52002delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.1006-131_1006-130delinsTC MANE Select ENSP00000357980.3:n.1006-131_1006-130delinsTC
ENST00000648167.1:c.688-131_688-130delinsTC ENSP00000498033.1:n.688-131_688-130delinsTC
ENST00000368984.7:c.1006-131_1006-130delinsTC ENSP00000357980.3:n.1006-131_1006-130delinsTC
ENST00000420892.1:c.229-131_229-130delinsTC ENSP00000412676.1:n.229-131_229-130delinsTC
NM_002775.4:c.1006-131_1006-130delinsTC NP_002766.1:n.1006-131_1006-130delinsTC
NM_002775.5:c.1006-131_1006-130delinsTC MANE Select NP_002766.1:n.1006-131_1006-130delinsTC