Canonical Allele Identifier: CA660871825
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs1279435415
MyVariant Identifiers: chr10:g.124231875_124231887del (hg19) chr10:g.122472359_122472371del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122472361_122472373del , CM000672.2:g.122472361_122472373del GRCh38
NC_000010.10:g.124231877_124231889del , CM000672.1:g.124231877_124231889del GRCh37
NC_000010.9:g.124221867_124221879del NCBI36
NG_011554.1:g.15837_15849del

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.472+10237_472+10249del MANE Select ENSP00000357980.3:n.472+10237_472+10249del
ENST00000648167.1:c.154+13652_154+13664del ENSP00000498033.1:n.154+13652_154+13664del
ENST00000368984.7:c.472+10237_472+10249del ENSP00000357980.3:n.472+10237_472+10249del
NM_002775.4:c.472+10237_472+10249del NP_002766.1:n.472+10237_472+10249del
NM_002775.5:c.472+10237_472+10249del MANE Select NP_002766.1:n.472+10237_472+10249del
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