Canonical Allele Identifier: CA471666729
Gene: HTRA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.124266260G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506744G>A , CM000672.2:g.122506744G>A GRCh38
NC_000010.10:g.124266260G>A , CM000672.1:g.124266260G>A GRCh37
NC_000010.9:g.124256250G>A NCBI36
NG_011554.1:g.50220G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.831G>A MANE Select ENSP00000357980.3:p.Glu277=
ENST00000648167.1:c.513G>A ENSP00000498033.1:p.Glu171=
ENST00000368984.7:c.831G>A ENSP00000357980.3:p.Glu277=
ENST00000420892.1:c.54G>A ENSP00000412676.1:p.Glu18=
NM_002775.4:c.831G>A NP_002766.1:p.Glu277=
NM_002775.5:c.831G>A MANE Select NP_002766.1:p.Glu277=
Search 100 bp 5'
Search 100 bp 3'