Canonical Allele Identifier: CA656509822

Gene: NOG

Linked Data

• COSMIC: COSN23580894

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56595115_56595116insG , CM000679.2:g.56595115_56595116insG	GRCh38
NC_000017.10:g.54672476_54672477insG , CM000679.1:g.54672476_54672477insG	GRCh37
NC_000017.9:g.52027475_52027476insG	NCBI36
NG_011958.1:g.6417_6418insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332822.6:c.*193_*194insG MANE Select	ENSP00000328181.4:n.*193_*194insG
ENST00000332822.4:c.*193_*194insG	ENSP00000328181.4:n.*193_*194insG
NM_005450.4:c.*193_*194insG	NP_005441.1:n.*193_*194insG
NM_005450.6:c.*193_*194insG MANE Select	NP_005441.1:n.*193_*194insG