Canonical Allele Identifier: CA645572368
Gene: NOG HGNC NCBI

Linked Data

COSMIC: COSM981625

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594638_56594646dup , CM000679.2:g.56594638_56594646dup GRCh38
NC_000017.10:g.54671999_54672007dup , CM000679.1:g.54671999_54672007dup GRCh37
NC_000017.9:g.52026998_52027006dup NCBI36
NG_011958.1:g.5940_5948dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.415_423dup MANE Select ENSP00000328181.4:p.Leu141_Arg142insLysLysLeu
ENST00000332822.4:c.415_423dup ENSP00000328181.4:p.Leu141_Arg142insLysLysLeu
NM_005450.4:c.415_423dup NP_005441.1:p.Leu141_Arg142insLysLysLeu
NM_005450.6:c.415_423dup MANE Select NP_005441.1:p.Leu141_Arg142insLysLysLeu