Canonical Allele Identifier: CA183538

Gene: NRAS

Linked Data

• ClinVar Variation Id: 179025
• ClinVar RCV Id: RCV000155806 ; RCV000373742 ; RCV000654962 ; RCV001261093 ; RCV003945240
• dbSNP Id: rs374061873
• ExAC: 1:115251173 G / A
• gnomAD v2: 1-115251173-G-A
• gnomAD v3: 1-114708552-G-A
• gnomAD v4: 1-114708552-G-A
• COSMIC: COSM327035
• MyVariant Identifiers: chr1:g.115251173G>A (hg19) ; chr1:g.114708552G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114708552G>A , CM000663.2:g.114708552G>A	GRCh38
NC_000001.10:g.115251173G>A , CM000663.1:g.115251173G>A	GRCh37
NC_000001.9:g.115052696G>A	NCBI36
NG_007572.1:g.13343C>T , LRG_92:g.13343C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.553C>T MANE Select	ENSP00000358548.4:p.Pro185Ser
ENST00000369535.4:c.553C>T	ENSP00000358548.4:p.Pro185Ser
NM_002524.4:c.553C>T	NP_002515.1:p.Pro185Ser
NM_002524.5:c.553C>T MANE Select	NP_002515.1:p.Pro185Ser