Canonical Allele Identifier: CA341741789

Gene: NRAS

Linked Data

• dbSNP Id: rs2101742161
• MyVariant Identifiers: chr1:g.115256585T>A (hg19) ; chr1:g.114713964T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114713964T>A , CM000663.2:g.114713964T>A	GRCh38
NC_000001.10:g.115256585T>A , CM000663.1:g.115256585T>A	GRCh37
NC_000001.9:g.115058108T>A	NCBI36
NG_007572.1:g.7931A>T , LRG_92:g.7931A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.126A>T MANE Select	ENSP00000358548.4:p.Lys42Asn
ENST00000369535.4:c.126A>T	ENSP00000358548.4:p.Lys42Asn
NM_002524.4:c.126A>T	NP_002515.1:p.Lys42Asn
NM_002524.5:c.126A>T MANE Select	NP_002515.1:p.Lys42Asn