Canonical Allele Identifier: CA1941477439

Gene: HTRA1

Linked Data

• dbSNP Id: rs2097503459
• gnomAD v4: 10-122507266-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.122507272dup , CM000672.2:g.122507272dup	GRCh38
NC_000010.10:g.124266788dup , CM000672.1:g.124266788dup	GRCh37
NC_000010.9:g.124256778dup	NCBI36
NG_011554.1:g.50748dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368984.8:c.973-98dup MANE Select	ENSP00000357980.3:n.973-98dup
ENST00000648167.1:c.655-98dup	ENSP00000498033.1:n.655-98dup
ENST00000368984.7:c.973-98dup	ENSP00000357980.3:n.973-98dup
ENST00000420892.1:c.196-98dup	ENSP00000412676.1:n.196-98dup
NM_002775.4:c.973-98dup	NP_002766.1:n.973-98dup
NM_002775.5:c.973-98dup MANE Select	NP_002766.1:n.973-98dup