Canonical Allele Identifier: CA1941477417
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122507199_122507202delinsATTG , CM000672.2:g.122507199_122507202delinsATTG GRCh38
NC_000010.10:g.124266715_124266718delinsATTG , CM000672.1:g.124266715_124266718delinsATTG GRCh37
NC_000010.9:g.124256705_124256708delinsATTG NCBI36
NG_011554.1:g.50675_50678delinsATTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.973-171_973-168delinsATTG MANE Select ENSP00000357980.3:n.973-171_973-168delinsATTG
ENST00000648167.1:c.655-171_655-168delinsATTG ENSP00000498033.1:n.655-171_655-168delinsATTG
ENST00000368984.7:c.973-171_973-168delinsATTG ENSP00000357980.3:n.973-171_973-168delinsATTG
ENST00000420892.1:c.196-171_196-168delinsATTG ENSP00000412676.1:n.196-171_196-168delinsATTG
NM_002775.4:c.973-171_973-168delinsATTG NP_002766.1:n.973-171_973-168delinsATTG
NM_002775.5:c.973-171_973-168delinsATTG MANE Select NP_002766.1:n.973-171_973-168delinsATTG