Canonical Allele Identifier: CA2611246766
Gene: HTRA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122507219_122507227del , CM000672.2:g.122507219_122507227del GRCh38
NC_000010.10:g.124266735_124266743del , CM000672.1:g.124266735_124266743del GRCh37
NC_000010.9:g.124256725_124256733del NCBI36
NG_011554.1:g.50695_50703del

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.973-151_973-143del MANE Select ENSP00000357980.3:n.973-151_973-143del
ENST00000648167.1:c.655-151_655-143del ENSP00000498033.1:n.655-151_655-143del
ENST00000368984.7:c.973-151_973-143del ENSP00000357980.3:n.973-151_973-143del
ENST00000420892.1:c.196-151_196-143del ENSP00000412676.1:n.196-151_196-143del
NM_002775.4:c.973-151_973-143del NP_002766.1:n.973-151_973-143del
NM_002775.5:c.973-151_973-143del MANE Select NP_002766.1:n.973-151_973-143del