Canonical Allele Identifier: CA1941478112
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122508728A= , CM000672.2:g.122508728A= GRCh38
NC_000010.10:g.124268244A= , CM000672.1:g.124268244A= GRCh37
NC_000010.9:g.124258234A= NCBI36
NG_011554.1:g.52204A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.1078A= MANE Select ENSP00000357980.3:p.Ile360=
ENST00000648167.1:c.760A= ENSP00000498033.1:p.Ile254=
ENST00000368984.7:c.1078A= ENSP00000357980.3:p.Ile360=
ENST00000420892.1:c.301A= ENSP00000412676.1:p.Ile101=
NM_002775.4:c.1078A= NP_002766.1:p.Ile360=
NM_002775.5:c.1078A= MANE Select NP_002766.1:p.Ile360=