Canonical Allele Identifier: CA1941477385
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122507141_122507142delinsCT , CM000672.2:g.122507141_122507142delinsCT GRCh38
NC_000010.10:g.124266657_124266658delinsCT , CM000672.1:g.124266657_124266658delinsCT GRCh37
NC_000010.9:g.124256647_124256648delinsCT NCBI36
NG_011554.1:g.50617_50618delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.973-229_973-228delinsCT MANE Select ENSP00000357980.3:n.973-229_973-228delinsCT
ENST00000648167.1:c.655-229_655-228delinsCT ENSP00000498033.1:n.655-229_655-228delinsCT
ENST00000368984.7:c.973-229_973-228delinsCT ENSP00000357980.3:n.973-229_973-228delinsCT
ENST00000420892.1:c.196-229_196-228delinsCT ENSP00000412676.1:n.196-229_196-228delinsCT
NM_002775.4:c.973-229_973-228delinsCT NP_002766.1:n.973-229_973-228delinsCT
NM_002775.5:c.973-229_973-228delinsCT MANE Select NP_002766.1:n.973-229_973-228delinsCT