Canonical Allele Identifier: CA471666553
Gene: HTRA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.124266212G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122506696G>A , CM000672.2:g.122506696G>A GRCh38
NC_000010.10:g.124266212G>A , CM000672.1:g.124266212G>A GRCh37
NC_000010.9:g.124256202G>A NCBI36
NG_011554.1:g.50172G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.783G>A MANE Select ENSP00000357980.3:p.Lys261=
ENST00000648167.1:c.465G>A ENSP00000498033.1:p.Lys155=
ENST00000368984.7:c.783G>A ENSP00000357980.3:p.Lys261=
ENST00000420892.1:c.6G>A ENSP00000412676.1:p.Lys2=
NM_002775.4:c.783G>A NP_002766.1:p.Lys261=
NM_002775.5:c.783G>A MANE Select NP_002766.1:p.Lys261=
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Search 100 bp 3'