Canonical Allele Identifier: CA2638881121
Gene: NOG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56595126_56595127insC , CM000679.2:g.56595126_56595127insC GRCh38
NC_000017.10:g.54672487_54672488insC , CM000679.1:g.54672487_54672488insC GRCh37
NC_000017.9:g.52027486_52027487insC NCBI36
NG_011958.1:g.6428_6429insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*204_*205insC MANE Select ENSP00000328181.4:n.*204_*205insC
ENST00000332822.4:c.*204_*205insC ENSP00000328181.4:n.*204_*205insC
NM_005450.4:c.*204_*205insC NP_005441.1:n.*204_*205insC
NM_005450.6:c.*204_*205insC MANE Select NP_005441.1:n.*204_*205insC