Canonical Allele Identifier: CA984892887

Gene: NOG

Linked Data

• dbSNP Id: rs2052474857
• gnomAD v3: 17-56595057-T-TTTTC
• gnomAD v4: 17-56595057-T-TTTTC

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56595057_56595058insTTTC , CM000679.2:g.56595057_56595058insTTTC	GRCh38
NC_000017.10:g.54672418_54672419insTTTC , CM000679.1:g.54672418_54672419insTTTC	GRCh37
NC_000017.9:g.52027417_52027418insTTTC	NCBI36
NG_011958.1:g.6359_6360insTTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332822.6:c.*135_*136insTTTC MANE Select	ENSP00000328181.4:n.*135_*136insTTTC
ENST00000332822.4:c.*135_*136insTTTC	ENSP00000328181.4:n.*135_*136insTTTC
NM_005450.4:c.*135_*136insTTTC	NP_005441.1:n.*135_*136insTTTC
NM_005450.6:c.*135_*136insTTTC MANE Select	NP_005441.1:n.*135_*136insTTTC