Canonical Allele Identifier: CA1020735

Gene: NRAS

Linked Data

• dbSNP Id: rs747960131
• ExAC: 1:115256377 G / T
• gnomAD v2: 1-115256377-G-T
• gnomAD v3: 1-114713756-G-T
• gnomAD v4: 1-114713756-G-T
• MyVariant Identifiers: chr1:g.115256377G>T (hg19) ; chr1:g.114713756G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114713756G>T , CM000663.2:g.114713756G>T	GRCh38
NC_000001.10:g.115256377G>T , CM000663.1:g.115256377G>T	GRCh37
NC_000001.9:g.115057900G>T	NCBI36
NG_007572.1:g.8139C>A , LRG_92:g.8139C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.290+44C>A MANE Select	ENSP00000358548.4:n.290+44C>A
ENST00000369535.4:c.290+44C>A	ENSP00000358548.4:n.290+44C>A
NM_002524.4:c.290+44C>A	NP_002515.1:n.290+44C>A
NM_002524.5:c.290+44C>A MANE Select	NP_002515.1:n.290+44C>A