Canonical Allele Identifier: CA1941477235
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506800T= , CM000672.2:g.122506800T= GRCh38
NC_000010.10:g.124266316T= , CM000672.1:g.124266316T= GRCh37
NC_000010.9:g.124256306T= NCBI36
NG_011554.1:g.50276T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.887T= MANE Select ENSP00000357980.3:p.Ile296=
ENST00000648167.1:c.569T= ENSP00000498033.1:p.Ile190=
ENST00000368984.7:c.887T= ENSP00000357980.3:p.Ile296=
ENST00000420892.1:c.110T= ENSP00000412676.1:p.Ile37=
NM_002775.4:c.887T= NP_002766.1:p.Ile296=
NM_002775.5:c.887T= MANE Select NP_002766.1:p.Ile296=