Canonical Allele Identifier: CA1941477131
Gene: HTRA1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506572C= , CM000672.2:g.122506572C= GRCh38
NC_000010.10:g.124266088C= , CM000672.1:g.124266088C= GRCh37
NC_000010.9:g.124256078C= NCBI36
NG_011554.1:g.50048C=

Transcript Alleles

HGVS Amino-acid change
ENST00000368984.8:c.778-119C= MANE Select ENSP00000357980.3:n.778-119C=
ENST00000648167.1:c.460-119C= ENSP00000498033.1:n.460-119C=
ENST00000368984.7:c.778-119C= ENSP00000357980.3:n.778-119C=
NM_002775.4:c.778-119C= NP_002766.1:n.778-119C=
NM_002775.5:c.778-119C= MANE Select NP_002766.1:n.778-119C=
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