Canonical Allele Identifier: CA471669051

Gene: HTRA1

Linked Data

• MyVariant Identifiers: chr10:g.124221522G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.122462006G>T , CM000672.2:g.122462006G>T	GRCh38
NC_000010.10:g.124221522G>T , CM000672.1:g.124221522G>T	GRCh37
NC_000010.9:g.124211512G>T	NCBI36
NG_011554.1:g.5482G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368984.8:c.354G>T MANE Select	ENSP00000357980.3:p.Val118=
ENST00000648167.1:c.154+3297G>T	ENSP00000498033.1:n.154+3297G>T
ENST00000368984.7:c.354G>T	ENSP00000357980.3:p.Val118=
NM_002775.4:c.354G>T	NP_002766.1:p.Val118=
NM_002775.5:c.354G>T MANE Select	NP_002766.1:p.Val118=