Canonical Allele Identifier: CA1941467410

Gene: HTRA1

Linked Data

• dbSNP Id: rs2097486374

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.122472130_122472132del , CM000672.2:g.122472130_122472132del	GRCh38
NC_000010.10:g.124231646_124231648del , CM000672.1:g.124231646_124231648del	GRCh37
NC_000010.9:g.124221636_124221638del	NCBI36
NG_011554.1:g.15606_15608del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368984.8:c.472+10006_472+10008del MANE Select	ENSP00000357980.3:n.472+10006_472+10008del
ENST00000648167.1:c.154+13421_154+13423del	ENSP00000498033.1:n.154+13421_154+13423del
ENST00000368984.7:c.472+10006_472+10008del	ENSP00000357980.3:n.472+10006_472+10008del
NM_002775.4:c.472+10006_472+10008del	NP_002766.1:n.472+10006_472+10008del
NM_002775.5:c.472+10006_472+10008del MANE Select	NP_002766.1:n.472+10006_472+10008del