Canonical Allele Identifier: CA1941477254
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506861C= , CM000672.2:g.122506861C= GRCh38
NC_000010.10:g.124266377C= , CM000672.1:g.124266377C= GRCh37
NC_000010.9:g.124256367C= NCBI36
NG_011554.1:g.50337C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.948C= MANE Select ENSP00000357980.3:p.Tyr316=
ENST00000648167.1:c.630C= ENSP00000498033.1:p.Tyr210=
ENST00000368984.7:c.948C= ENSP00000357980.3:p.Tyr316=
ENST00000420892.1:c.171C= ENSP00000412676.1:p.Tyr57=
NM_002775.4:c.948C= NP_002766.1:p.Tyr316=
NM_002775.5:c.948C= MANE Select NP_002766.1:p.Tyr316=