Canonical Allele Identifier: CA1941459145
Gene: HTRA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461601C= , CM000672.2:g.122461601C= GRCh38
NC_000010.10:g.124221117C= , CM000672.1:g.124221117C= GRCh37
NC_000010.9:g.124211107C= NCBI36
NG_011554.1:g.5077C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.-52C= MANE Select ENSP00000357980.3:n.-52C=
ENST00000648167.1:c.154+2892C= ENSP00000498033.1:n.154+2892C=
ENST00000368984.7:c.-52C= ENSP00000357980.3:n.-52C=
NM_002775.4:c.-52C= NP_002766.1:n.-52C=
NM_002775.5:c.-52C= MANE Select NP_002766.1:n.-52C=