Canonical Allele Identifier: CA660871894
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs1333811124
MyVariant Identifiers: chr10:g.124231894_124231895insTAC (hg19) chr10:g.122472378_122472379insTAC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122472380_122472381insCTA , CM000672.2:g.122472380_122472381insCTA GRCh38
NC_000010.10:g.124231896_124231897insCTA , CM000672.1:g.124231896_124231897insCTA GRCh37
NC_000010.9:g.124221886_124221887insCTA NCBI36
NG_011554.1:g.15856_15857insCTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.472+10256_472+10257insCTA MANE Select ENSP00000357980.3:n.472+10256_472+10257insCTA
ENST00000648167.1:c.154+13671_154+13672insCTA ENSP00000498033.1:n.154+13671_154+13672insCTA
ENST00000368984.7:c.472+10256_472+10257insCTA ENSP00000357980.3:n.472+10256_472+10257insCTA
NM_002775.4:c.472+10256_472+10257insCTA NP_002766.1:n.472+10256_472+10257insCTA
NM_002775.5:c.472+10256_472+10257insCTA MANE Select NP_002766.1:n.472+10256_472+10257insCTA
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