Canonical Allele Identifier: CA933343458
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs900990758

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122472369_122472377dup , CM000672.2:g.122472369_122472377dup GRCh38
NC_000010.10:g.124231885_124231893dup , CM000672.1:g.124231885_124231893dup GRCh37
NC_000010.9:g.124221875_124221883dup NCBI36
NG_011554.1:g.15845_15853dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.472+10245_472+10253dup MANE Select ENSP00000357980.3:n.472+10245_472+10253dup
ENST00000648167.1:c.154+13660_154+13668dup ENSP00000498033.1:n.154+13660_154+13668dup
ENST00000368984.7:c.472+10245_472+10253dup ENSP00000357980.3:n.472+10245_472+10253dup
NM_002775.4:c.472+10245_472+10253dup NP_002766.1:n.472+10245_472+10253dup
NM_002775.5:c.472+10245_472+10253dup MANE Select NP_002766.1:n.472+10245_472+10253dup