Canonical Allele Identifier: CA10607700

Gene: NRAS

Linked Data

• ClinVar Variation Id: 291975
• ClinVar RCV Id: RCV000317051 ; RCV003409431
• dbSNP Id: rs188272768
• gnomAD v2: 1-115250604-T-C
• gnomAD v3: 1-114707983-T-C
• gnomAD v4: 1-114707983-T-C
• MyVariant Identifiers: chr1:g.115250604T>C (hg19) ; chr1:g.114707983T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114707983T>C , CM000663.2:g.114707983T>C	GRCh38
NC_000001.10:g.115250604T>C , CM000663.1:g.115250604T>C	GRCh37
NC_000001.9:g.115052127T>C	NCBI36
NG_007572.1:g.13912A>G , LRG_92:g.13912A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.*111A>G MANE Select	ENSP00000358548.4:n.*111A>G
ENST00000369535.4:c.*111A>G	ENSP00000358548.4:n.*111A>G
NM_002524.4:c.*111A>G	NP_002515.1:n.*111A>G
NM_002524.5:c.*111A>G MANE Select	NP_002515.1:n.*111A>G