Canonical Allele Identifier: CA214415103
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs777317444
gnomAD v2: 10-124221145-A-ACCG
gnomAD v3: 10-122461629-A-ACCG
gnomAD v4: 10-122461629-A-ACCG
MyVariant Identifiers: chr10:g.124221148_124221149insCCG (hg19) chr10:g.124221145_124221146insCCG (hg19) chr10:g.122461629_122461630insCCG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461641_122461643dup , CM000672.2:g.122461641_122461643dup GRCh38
NC_000010.10:g.124221157_124221159dup , CM000672.1:g.124221157_124221159dup GRCh37
NC_000010.9:g.124211147_124211149dup NCBI36
NG_011554.1:g.5117_5119dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.-12_-10dup MANE Select ENSP00000357980.3:n.-12_-10dup
ENST00000648167.1:c.154+2932_154+2934dup ENSP00000498033.1:n.154+2932_154+2934dup
ENST00000368984.7:c.-12_-10dup ENSP00000357980.3:n.-12_-10dup
NM_002775.4:c.-12_-10dup NP_002766.1:n.-12_-10dup
NM_002775.5:c.-12_-10dup MANE Select NP_002766.1:n.-12_-10dup
Search 100 bp 5'
Search 100 bp 3'