Canonical Allele Identifier: CA471666972

Gene: HTRA1

Linked Data

• MyVariant Identifiers: chr10:g.124266359C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.122506843C>T , CM000672.2:g.122506843C>T	GRCh38
NC_000010.10:g.124266359C>T , CM000672.1:g.124266359C>T	GRCh37
NC_000010.9:g.124256349C>T	NCBI36
NG_011554.1:g.50319C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368984.8:c.930C>T MANE Select	ENSP00000357980.3:p.Arg310=
ENST00000648167.1:c.612C>T	ENSP00000498033.1:p.Arg204=
ENST00000368984.7:c.930C>T	ENSP00000357980.3:p.Arg310=
ENST00000420892.1:c.153C>T	ENSP00000412676.1:p.Arg51=
NM_002775.4:c.930C>T	NP_002766.1:p.Arg310=
NM_002775.5:c.930C>T MANE Select	NP_002766.1:p.Arg310=