Canonical Allele Identifier: CA471666764

Gene: HTRA1

Linked Data

• MyVariant Identifiers: chr10:g.124266272C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.122506756C>G , CM000672.2:g.122506756C>G	GRCh38
NC_000010.10:g.124266272C>G , CM000672.1:g.124266272C>G	GRCh37
NC_000010.9:g.124256262C>G	NCBI36
NG_011554.1:g.50232C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368984.8:c.843C>G MANE Select	ENSP00000357980.3:p.Ala281=
ENST00000648167.1:c.525C>G	ENSP00000498033.1:p.Ala175=
ENST00000368984.7:c.843C>G	ENSP00000357980.3:p.Ala281=
ENST00000420892.1:c.66C>G	ENSP00000412676.1:p.Ala22=
NM_002775.4:c.843C>G	NP_002766.1:p.Ala281=
NM_002775.5:c.843C>G MANE Select	NP_002766.1:p.Ala281=