Canonical Allele Identifier: CA596578963
Gene: HTRA1 HGNC NCBI

Linked Data

dbSNP Id: rs1285111587
gnomAD v2: 10-124221102-C-CCTG
MyVariant Identifiers: chr10:g.124221102_124221103insCTG (hg19) chr10:g.122461586_122461587insCTG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.122461586_122461587insCTG , CM000672.2:g.122461586_122461587insCTG GRCh38
NC_000010.10:g.124221102_124221103insCTG , CM000672.1:g.124221102_124221103insCTG GRCh37
NC_000010.9:g.124211092_124211093insCTG NCBI36
NG_011554.1:g.5062_5063insCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000368984.8:c.-67_-66insCTG MANE Select ENSP00000357980.3:n.-67_-66insCTG
ENST00000648167.1:c.154+2877_154+2878insCTG ENSP00000498033.1:n.154+2877_154+2878insCTG
ENST00000368984.7:c.-67_-66insCTG ENSP00000357980.3:n.-67_-66insCTG
NM_002775.4:c.-67_-66insCTG NP_002766.1:n.-67_-66insCTG
NM_002775.5:c.-67_-66insCTG MANE Select NP_002766.1:n.-67_-66insCTG
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