Canonical Allele Identifier: CA471745315

Gene: HTRA1

Linked Data

• gnomAD v4: 10-122461683-C-T
• MyVariant Identifiers: chr10:g.124221199C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.122461683C>T , CM000672.2:g.122461683C>T	GRCh38
NC_000010.10:g.124221199C>T , CM000672.1:g.124221199C>T	GRCh37
NC_000010.9:g.124211189C>T	NCBI36
NG_011554.1:g.5159C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368984.8:c.31C>T MANE Select	ENSP00000357980.3:p.Leu11=
ENST00000648167.1:c.154+2974C>T	ENSP00000498033.1:n.154+2974C>T
ENST00000368984.7:c.31C>T	ENSP00000357980.3:p.Leu11=
NM_002775.4:c.31C>T	NP_002766.1:p.Leu11=
NM_002775.5:c.31C>T MANE Select	NP_002766.1:p.Leu11=