Canonical Allele Identifier: CA1941477270
Gene: HTRA1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506892C= , CM000672.2:g.122506892C= GRCh38
NC_000010.10:g.124266408C= , CM000672.1:g.124266408C= GRCh37
NC_000010.9:g.124256398C= NCBI36
NG_011554.1:g.50368C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.972+7C= MANE Select ENSP00000357980.3:n.972+7C=
ENST00000648167.1:c.654+7C= ENSP00000498033.1:n.654+7C=
ENST00000368984.7:c.972+7C= ENSP00000357980.3:n.972+7C=
ENST00000420892.1:c.195+7C= ENSP00000412676.1:n.195+7C=
NM_002775.4:c.972+7C= NP_002766.1:n.972+7C=
NM_002775.5:c.972+7C= MANE Select NP_002766.1:n.972+7C=
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