Canonical Allele Identifier: CA984892871

Gene: NOG

Linked Data

• dbSNP Id: rs2052474752
• gnomAD v3: 17-56595055-TTTC-T
• gnomAD v4: 17-56595055-TTTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56595057_56595059del , CM000679.2:g.56595057_56595059del	GRCh38
NC_000017.10:g.54672418_54672420del , CM000679.1:g.54672418_54672420del	GRCh37
NC_000017.9:g.52027417_52027419del	NCBI36
NG_011958.1:g.6359_6361del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000332822.6:c.*135_*137del MANE Select	ENSP00000328181.4:n.*135_*137del
ENST00000332822.4:c.*135_*137del	ENSP00000328181.4:n.*135_*137del
NM_005450.4:c.*135_*137del	NP_005441.1:n.*135_*137del
NM_005450.6:c.*135_*137del MANE Select	NP_005441.1:n.*135_*137del