Canonical Allele Identifier: CA1941467545

Gene: HTRA1

Linked Data

• dbSNP Id: rs2097486509

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.122472370_122472371insGTT , CM000672.2:g.122472370_122472371insGTT	GRCh38
NC_000010.10:g.124231886_124231887insGTT , CM000672.1:g.124231886_124231887insGTT	GRCh37
NC_000010.9:g.124221876_124221877insGTT	NCBI36
NG_011554.1:g.15846_15847insGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368984.8:c.472+10246_472+10247insGTT MANE Select	ENSP00000357980.3:n.472+10246_472+10247insGTT
ENST00000648167.1:c.154+13661_154+13662insGTT	ENSP00000498033.1:n.154+13661_154+13662insGTT
ENST00000368984.7:c.472+10246_472+10247insGTT	ENSP00000357980.3:n.472+10246_472+10247insGTT
NM_002775.4:c.472+10246_472+10247insGTT	NP_002766.1:n.472+10246_472+10247insGTT
NM_002775.5:c.472+10246_472+10247insGTT MANE Select	NP_002766.1:n.472+10246_472+10247insGTT