Canonical Allele Identifier: CA1941478154

Gene: HTRA1

Linked Data

• dbSNP Id: rs2097504319

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.122508807_122508808insGCTCAGCTGCCCTT , CM000672.2:g.122508807_122508808insGCTCAGCTGCCCTT	GRCh38
NC_000010.10:g.124268323_124268324insGCTCAGCTGCCCTT , CM000672.1:g.124268323_124268324insGCTCAGCTGCCCTT	GRCh37
NC_000010.9:g.124258313_124258314insGCTCAGCTGCCCTT	NCBI36
NG_011554.1:g.52283_52284insGCTCAGCTGCCCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368984.8:c.1120+37_1120+38insGCTCAGCTGCCCTT MANE Select	ENSP00000357980.3:n.1120+37_1120+38insGCTCAGCTGCCCTT
ENST00000648167.1:c.802+37_802+38insGCTCAGCTGCCCTT	ENSP00000498033.1:n.802+37_802+38insGCTCAGCTGCCCTT
ENST00000368984.7:c.1120+37_1120+38insGCTCAGCTGCCCTT	ENSP00000357980.3:n.1120+37_1120+38insGCTCAGCTGCCCTT
ENST00000420892.1:c.343+37_343+38insGCTCAGCTGCCCTT	ENSP00000412676.1:n.343+37_343+38insGCTCAGCTGCCCTT
NM_002775.4:c.1120+37_1120+38insGCTCAGCTGCCCTT	NP_002766.1:n.1120+37_1120+38insGCTCAGCTGCCCTT
NM_002775.5:c.1120+37_1120+38insGCTCAGCTGCCCTT MANE Select	NP_002766.1:n.1120+37_1120+38insGCTCAGCTGCCCTT