Canonical Allele Identifier: CA1941477277
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506916_122506917delinsTG , CM000672.2:g.122506916_122506917delinsTG GRCh38
NC_000010.10:g.124266432_124266433delinsTG , CM000672.1:g.124266432_124266433delinsTG GRCh37
NC_000010.9:g.124256422_124256423delinsTG NCBI36
NG_011554.1:g.50392_50393delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.972+31_972+32delinsTG MANE Select ENSP00000357980.3:n.972+31_972+32delinsTG
ENST00000648167.1:c.654+31_654+32delinsTG ENSP00000498033.1:n.654+31_654+32delinsTG
ENST00000368984.7:c.972+31_972+32delinsTG ENSP00000357980.3:n.972+31_972+32delinsTG
ENST00000420892.1:c.195+31_195+32delinsTG ENSP00000412676.1:n.195+31_195+32delinsTG
NM_002775.4:c.972+31_972+32delinsTG NP_002766.1:n.972+31_972+32delinsTG
NM_002775.5:c.972+31_972+32delinsTG MANE Select NP_002766.1:n.972+31_972+32delinsTG