Canonical Allele Identifier: CA29040498
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs999453042
MyVariant Identifiers: chr1:g.115249361_115249375del (hg19) chr1:g.114706740_114706754del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114706740_114706754del , CM000663.2:g.114706740_114706754del GRCh38
NC_000001.10:g.115249361_115249375del , CM000663.1:g.115249361_115249375del GRCh37
NC_000001.9:g.115050884_115050898del NCBI36
NG_007572.1:g.15141_15155del , LRG_92:g.15141_15155del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*1340_*1354del MANE Select ENSP00000358548.4:n.*1340_*1354del
ENST00000369535.4:c.*1340_*1354del ENSP00000358548.4:n.*1340_*1354del
NM_002524.4:c.*1340_*1354del NP_002515.1:n.*1340_*1354del
NM_002524.5:c.*1340_*1354del MANE Select NP_002515.1:n.*1340_*1354del
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