Canonical Allele Identifier: CA471667168
Gene: HTRA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.124268285A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122508769A>G , CM000672.2:g.122508769A>G GRCh38
NC_000010.10:g.124268285A>G , CM000672.1:g.124268285A>G GRCh37
NC_000010.9:g.124258275A>G NCBI36
NG_011554.1:g.52245A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000368984.8:c.1119A>G MANE Select ENSP00000357980.3:p.Lys373=
ENST00000648167.1:c.801A>G ENSP00000498033.1:p.Lys267=
ENST00000368984.7:c.1119A>G ENSP00000357980.3:p.Lys373=
ENST00000420892.1:c.342A>G ENSP00000412676.1:p.Lys114=
NM_002775.4:c.1119A>G NP_002766.1:p.Lys373=
NM_002775.5:c.1119A>G MANE Select NP_002766.1:p.Lys373=