Canonical Allele Identifier: CA2611246996
Gene: HTRA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122508598_122508599insAA , CM000672.2:g.122508598_122508599insAA GRCh38
NC_000010.10:g.124268114_124268115insAA , CM000672.1:g.124268114_124268115insAA GRCh37
NC_000010.9:g.124258104_124258105insAA NCBI36
NG_011554.1:g.52074_52075insAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.1006-58_1006-57insAA MANE Select ENSP00000357980.3:n.1006-58_1006-57insAA
ENST00000648167.1:c.688-58_688-57insAA ENSP00000498033.1:n.688-58_688-57insAA
ENST00000368984.7:c.1006-58_1006-57insAA ENSP00000357980.3:n.1006-58_1006-57insAA
ENST00000420892.1:c.229-58_229-57insAA ENSP00000412676.1:n.229-58_229-57insAA
NM_002775.4:c.1006-58_1006-57insAA NP_002766.1:n.1006-58_1006-57insAA
NM_002775.5:c.1006-58_1006-57insAA MANE Select NP_002766.1:n.1006-58_1006-57insAA