Canonical Allele Identifier: CA773336810
Gene: NOG HGNC NCBI

Linked Data

dbSNP Id: rs1341935735
gnomAD v3: 17-56594927-CG-C
gnomAD v4: 17-56594927-CG-C
MyVariant Identifiers: chr17:g.54672289del (hg19) chr17:g.56594928del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594932del , CM000679.2:g.56594932del GRCh38
NC_000017.10:g.54672293del , CM000679.1:g.54672293del GRCh37
NC_000017.9:g.52027292del NCBI36
NG_011958.1:g.6234del

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*10del MANE Select ENSP00000328181.4:n.*10del
ENST00000332822.4:c.*10del ENSP00000328181.4:n.*10del
NM_005450.4:c.*10del NP_005441.1:n.*10del
NM_005450.6:c.*10del MANE Select NP_005441.1:n.*10del
Search 100 bp 5'
Search 100 bp 3'