Canonical Allele Identifier: CA2266876479
Gene: NOG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56595029_56595031delinsAAC , CM000679.2:g.56595029_56595031delinsAAC GRCh38
NC_000017.10:g.54672390_54672392delinsAAC , CM000679.1:g.54672390_54672392delinsAAC GRCh37
NC_000017.9:g.52027389_52027391delinsAAC NCBI36
NG_011958.1:g.6331_6333delinsAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*107_*109delinsAAC MANE Select ENSP00000328181.4:n.*107_*109delinsAAC
ENST00000332822.4:c.*107_*109delinsAAC ENSP00000328181.4:n.*107_*109delinsAAC
NM_005450.4:c.*107_*109delinsAAC NP_005441.1:n.*107_*109delinsAAC
NM_005450.6:c.*107_*109delinsAAC MANE Select NP_005441.1:n.*107_*109delinsAAC