Canonical Allele Identifier: CA2266876488
Gene: NOG HGNC NCBI

Linked Data

dbSNP Id: rs2052474115

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56595030_56595031insATTT , CM000679.2:g.56595030_56595031insATTT GRCh38
NC_000017.10:g.54672391_54672392insATTT , CM000679.1:g.54672391_54672392insATTT GRCh37
NC_000017.9:g.52027390_52027391insATTT NCBI36
NG_011958.1:g.6332_6333insATTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*108_*109insATTT MANE Select ENSP00000328181.4:n.*108_*109insATTT
ENST00000332822.4:c.*108_*109insATTT ENSP00000328181.4:n.*108_*109insATTT
NM_005450.4:c.*108_*109insATTT NP_005441.1:n.*108_*109insATTT
NM_005450.6:c.*108_*109insATTT MANE Select NP_005441.1:n.*108_*109insATTT