Canonical Allele Identifier: CA378606398
Gene: HTRA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122462079C>G , CM000672.2:g.122462079C>G GRCh38
NC_000010.10:g.124221595C>G , CM000672.1:g.124221595C>G GRCh37
NC_000010.9:g.124211585C>G NCBI36
NG_011554.1:g.5555C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.427C>G MANE Select ENSP00000357980.3:p.His143Asp
ENST00000648167.1:c.154+3370C>G ENSP00000498033.1:n.154+3370C>G
ENST00000368984.7:c.427C>G ENSP00000357980.3:p.His143Asp
NM_002775.4:c.427C>G NP_002766.1:p.His143Asp
NM_002775.5:c.427C>G MANE Select NP_002766.1:p.His143Asp