Canonical Allele Identifier: CA1941478057
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122508557G= , CM000672.2:g.122508557G= GRCh38
NC_000010.10:g.124268073G= , CM000672.1:g.124268073G= GRCh37
NC_000010.9:g.124258063G= NCBI36
NG_011554.1:g.52033G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.1006-99G= MANE Select ENSP00000357980.3:n.1006-99G=
ENST00000648167.1:c.688-99G= ENSP00000498033.1:n.688-99G=
ENST00000368984.7:c.1006-99G= ENSP00000357980.3:n.1006-99G=
ENST00000420892.1:c.229-99G= ENSP00000412676.1:n.229-99G=
NM_002775.4:c.1006-99G= NP_002766.1:n.1006-99G=
NM_002775.5:c.1006-99G= MANE Select NP_002766.1:n.1006-99G=