Canonical Allele Identifier: CA1941477190
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506707T= , CM000672.2:g.122506707T= GRCh38
NC_000010.10:g.124266223T= , CM000672.1:g.124266223T= GRCh37
NC_000010.9:g.124256213T= NCBI36
NG_011554.1:g.50183T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.794T= MANE Select ENSP00000357980.3:p.Leu265=
ENST00000648167.1:c.476T= ENSP00000498033.1:p.Leu159=
ENST00000368984.7:c.794T= ENSP00000357980.3:p.Leu265=
ENST00000420892.1:c.17T= ENSP00000412676.1:p.Leu6=
NM_002775.4:c.794T= NP_002766.1:p.Leu265=
NM_002775.5:c.794T= MANE Select NP_002766.1:p.Leu265=