Canonical Allele Identifier: CA10607485

Gene: NRAS

Linked Data

• ClinVar Variation Id: 291966
• ClinVar RCV Id: RCV000307322
• dbSNP Id: rs886045106
• MyVariant Identifiers: chr1:g.115249780dupT (hg19) ; chr1:g.115249779_115249780insT (hg19) ; chr1:g.114707159dupT (hg38) ; chr1:g.114707158_114707159insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114707159dup , CM000663.2:g.114707159dup	GRCh38
NC_000001.10:g.115249780dup , CM000663.1:g.115249780dup	GRCh37
NC_000001.9:g.115051303dup	NCBI36
NG_007572.1:g.14736dup , LRG_92:g.14736dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000369535.5:c.*935dup MANE Select	ENSP00000358548.4:n.*935dup
ENST00000369535.4:c.*935dup	ENSP00000358548.4:n.*935dup
NM_002524.4:c.*935dup	NP_002515.1:n.*935dup
NM_002524.5:c.*935dup MANE Select	NP_002515.1:n.*935dup