Canonical Allele Identifier: CA2638881038

Gene: NOG

Linked Data

• gnomAD v4: 17-56595030-A-ATTT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56595030_56595031insTTT , CM000679.2:g.56595030_56595031insTTT	GRCh38
NC_000017.10:g.54672391_54672392insTTT , CM000679.1:g.54672391_54672392insTTT	GRCh37
NC_000017.9:g.52027390_52027391insTTT	NCBI36
NG_011958.1:g.6332_6333insTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332822.6:c.*108_*109insTTT MANE Select	ENSP00000328181.4:n.*108_*109insTTT
ENST00000332822.4:c.*108_*109insTTT	ENSP00000328181.4:n.*108_*109insTTT
NM_005450.4:c.*108_*109insTTT	NP_005441.1:n.*108_*109insTTT
NM_005450.6:c.*108_*109insTTT MANE Select	NP_005441.1:n.*108_*109insTTT