Canonical Allele Identifier: CA1941477249
Gene: HTRA1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506842G= , CM000672.2:g.122506842G= GRCh38
NC_000010.10:g.124266358G= , CM000672.1:g.124266358G= GRCh37
NC_000010.9:g.124256348G= NCBI36
NG_011554.1:g.50318G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.929G= MANE Select ENSP00000357980.3:p.Arg310=
ENST00000648167.1:c.611G= ENSP00000498033.1:p.Arg204=
ENST00000368984.7:c.929G= ENSP00000357980.3:p.Arg310=
ENST00000420892.1:c.152G= ENSP00000412676.1:p.Arg51=
NM_002775.4:c.929G= NP_002766.1:p.Arg310=
NM_002775.5:c.929G= MANE Select NP_002766.1:p.Arg310=
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