Canonical Allele Identifier: CA471667147
Gene: HTRA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.124268243G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122508727G>A , CM000672.2:g.122508727G>A GRCh38
NC_000010.10:g.124268243G>A , CM000672.1:g.124268243G>A GRCh37
NC_000010.9:g.124258233G>A NCBI36
NG_011554.1:g.52203G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.1077G>A MANE Select ENSP00000357980.3:p.Lys359=
ENST00000648167.1:c.759G>A ENSP00000498033.1:p.Lys253=
ENST00000368984.7:c.1077G>A ENSP00000357980.3:p.Lys359=
ENST00000420892.1:c.300G>A ENSP00000412676.1:p.Lys100=
NM_002775.4:c.1077G>A NP_002766.1:p.Lys359=
NM_002775.5:c.1077G>A MANE Select NP_002766.1:p.Lys359=
Search 100 bp 5'
Search 100 bp 3'