Canonical Allele Identifier: CA773337105
Gene: NOG HGNC NCBI

Linked Data

dbSNP Id: rs1213746413
gnomAD v3: 17-56595175-T-TA
gnomAD v4: 17-56595175-T-TA
MyVariant Identifiers: chr17:g.54672536_54672537insA (hg19) chr17:g.56595175_56595176insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56595176dup , CM000679.2:g.56595176dup GRCh38
NC_000017.10:g.54672537dup , CM000679.1:g.54672537dup GRCh37
NC_000017.9:g.52027536dup NCBI36
NG_011958.1:g.6478dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*254dup MANE Select ENSP00000328181.4:n.*254dup
ENST00000332822.4:c.*254dup ENSP00000328181.4:n.*254dup
NM_005450.4:c.*254dup NP_005441.1:n.*254dup
NM_005450.6:c.*254dup MANE Select NP_005441.1:n.*254dup
Search 100 bp 5'
Search 100 bp 3'