Canonical Allele Identifier: CA297029

Gene: NRAS

Linked Data

• ClinVar Variation Id: 40472
• ClinVar RCV Id: RCV000158984
• dbSNP Id: rs730880967
• MyVariant Identifiers: chr1:g.115256598_115256600dupTCC (hg19) ; chr1:g.115256597_115256598insTCC (hg19) ; chr1:g.114713977_114713979dupTCC (hg38) ; chr1:g.114713976_114713977insTCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114713978_114713980dup , CM000663.2:g.114713978_114713980dup	GRCh38
NC_000001.10:g.115256599_115256601dup , CM000663.1:g.115256599_115256601dup	GRCh37
NC_000001.9:g.115058122_115058124dup	NCBI36
NG_007572.1:g.7916_7918dup , LRG_92:g.7916_7918dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.112-1_113dup
ENST00000369535.4:c.112-1_113dup
NM_002524.4:c.112-1_113dup
NM_002524.5:c.112-1_113dup