Canonical Allele Identifier: CA2647248592

Gene: NRAS

Linked Data

• gnomAD v4: 1-114714008-A-AAGGGGGGCTGGGT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114714008_114714009insAGGGGGGCTGGGT , CM000663.2:g.114714008_114714009insAGGGGGGCTGGGT	GRCh38
NC_000001.10:g.115256629_115256630insAGGGGGGCTGGGT , CM000663.1:g.115256629_115256630insAGGGGGGCTGGGT	GRCh37
NC_000001.9:g.115058152_115058153insAGGGGGGCTGGGT	NCBI36
NG_007572.1:g.7886_7887insACCCAGCCCCCCT , LRG_92:g.7886_7887insACCCAGCCCCCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.112-31_112-30insACCCAGCCCCCCT MANE Select	ENSP00000358548.4:n.112-31_112-30insACCCAGCCCCCCT
ENST00000369535.4:c.112-31_112-30insACCCAGCCCCCCT	ENSP00000358548.4:n.112-31_112-30insACCCAGCCCCCCT
NM_002524.4:c.112-31_112-30insACCCAGCCCCCCT	NP_002515.1:n.112-31_112-30insACCCAGCCCCCCT
NM_002524.5:c.112-31_112-30insACCCAGCCCCCCT MANE Select	NP_002515.1:n.112-31_112-30insACCCAGCCCCCCT