Canonical Allele Identifier: CA1941478107
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122508715C= , CM000672.2:g.122508715C= GRCh38
NC_000010.10:g.124268231C= , CM000672.1:g.124268231C= GRCh37
NC_000010.9:g.124258221C= NCBI36
NG_011554.1:g.52191C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.1065C= MANE Select ENSP00000357980.3:p.Ile355=
ENST00000648167.1:c.747C= ENSP00000498033.1:p.Ile249=
ENST00000368984.7:c.1065C= ENSP00000357980.3:p.Ile355=
ENST00000420892.1:c.288C= ENSP00000412676.1:p.Ile96=
NM_002775.4:c.1065C= NP_002766.1:p.Ile355=
NM_002775.5:c.1065C= MANE Select NP_002766.1:p.Ile355=