Canonical Allele Identifier: CA471666660

Gene: HTRA1

Linked Data

• MyVariant Identifiers: chr10:g.124266242A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.122506726A>G , CM000672.2:g.122506726A>G	GRCh38
NC_000010.10:g.124266242A>G , CM000672.1:g.124266242A>G	GRCh37
NC_000010.9:g.124256232A>G	NCBI36
NG_011554.1:g.50202A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368984.8:c.813A>G MANE Select	ENSP00000357980.3:p.Ser271=
ENST00000648167.1:c.495A>G	ENSP00000498033.1:p.Ser165=
ENST00000368984.7:c.813A>G	ENSP00000357980.3:p.Ser271=
ENST00000420892.1:c.36A>G	ENSP00000412676.1:p.Ser12=
NM_002775.4:c.813A>G	NP_002766.1:p.Ser271=
NM_002775.5:c.813A>G MANE Select	NP_002766.1:p.Ser271=