Canonical Allele Identifier: CA341741430

Gene: NRAS

Linked Data

• dbSNP Id: rs2101741820
• MyVariant Identifiers: chr1:g.115256456A>T (hg19) ; chr1:g.114713835A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114713835A>T , CM000663.2:g.114713835A>T	GRCh38
NC_000001.10:g.115256456A>T , CM000663.1:g.115256456A>T	GRCh37
NC_000001.9:g.115057979A>T	NCBI36
NG_007572.1:g.8060T>A , LRG_92:g.8060T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.255T>A MANE Select	ENSP00000358548.4:p.Asn85Lys
ENST00000369535.4:c.255T>A	ENSP00000358548.4:p.Asn85Lys
NM_002524.4:c.255T>A	NP_002515.1:p.Asn85Lys
NM_002524.5:c.255T>A MANE Select	NP_002515.1:p.Asn85Lys