Canonical Allele Identifier: CA471667110

Gene: HTRA1

Linked Data

• MyVariant Identifiers: chr10:g.124268195C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.122508679C>T , CM000672.2:g.122508679C>T	GRCh38
NC_000010.10:g.124268195C>T , CM000672.1:g.124268195C>T	GRCh37
NC_000010.9:g.124258185C>T	NCBI36
NG_011554.1:g.52155C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368984.8:c.1029C>T MANE Select	ENSP00000357980.3:p.Asn343=
ENST00000648167.1:c.711C>T	ENSP00000498033.1:p.Asn237=
ENST00000368984.7:c.1029C>T	ENSP00000357980.3:p.Asn343=
ENST00000420892.1:c.252C>T	ENSP00000412676.1:p.Asn84=
NM_002775.4:c.1029C>T	NP_002766.1:p.Asn343=
NM_002775.5:c.1029C>T MANE Select	NP_002766.1:p.Asn343=