Canonical Allele Identifier: CA399967016
Gene: NOG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594919C>A , CM000679.2:g.56594919C>A GRCh38
NC_000017.10:g.54672280C>A , CM000679.1:g.54672280C>A GRCh37
NC_000017.9:g.52027279C>A NCBI36
NG_011958.1:g.6221C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.696C>A MANE Select ENSP00000328181.4:p.Cys232Ter
ENST00000332822.4:c.696C>A ENSP00000328181.4:p.Cys232Ter
NM_005450.4:c.696C>A NP_005441.1:p.Cys232Ter
NM_005450.6:c.696C>A MANE Select NP_005441.1:p.Cys232Ter