Canonical Allele Identifier: CA2595867855
Gene: NOG HGNC NCBI

Linked Data

dbSNP Id: rs2145567719

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594975_56594976insT , CM000679.2:g.56594975_56594976insT GRCh38
NC_000017.10:g.54672336_54672337insT , CM000679.1:g.54672336_54672337insT GRCh37
NC_000017.9:g.52027335_52027336insT NCBI36
NG_011958.1:g.6277_6278insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.*53_*54insT MANE Select ENSP00000328181.4:n.*53_*54insT
ENST00000332822.4:c.*53_*54insT ENSP00000328181.4:n.*53_*54insT
NM_005450.4:c.*53_*54insT NP_005441.1:n.*53_*54insT
NM_005450.6:c.*53_*54insT MANE Select NP_005441.1:n.*53_*54insT