Canonical Allele Identifier: CA471666820

Gene: HTRA1

Linked Data

• MyVariant Identifiers: chr10:g.124266290C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.122506774C>G , CM000672.2:g.122506774C>G	GRCh38
NC_000010.10:g.124266290C>G , CM000672.1:g.124266290C>G	GRCh37
NC_000010.9:g.124256280C>G	NCBI36
NG_011554.1:g.50250C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368984.8:c.861C>G MANE Select	ENSP00000357980.3:p.Ser287=
ENST00000648167.1:c.543C>G	ENSP00000498033.1:p.Ser181=
ENST00000368984.7:c.861C>G	ENSP00000357980.3:p.Ser287=
ENST00000420892.1:c.84C>G	ENSP00000412676.1:p.Ser28=
NM_002775.4:c.861C>G	NP_002766.1:p.Ser287=
NM_002775.5:c.861C>G MANE Select	NP_002766.1:p.Ser287=