Canonical Allele Identifier: CA1190286051

Gene: NRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114707684_114707686delinsGAA , CM000663.2:g.114707684_114707686delinsGAA	GRCh38
NC_000001.10:g.115250305_115250307delinsGAA , CM000663.1:g.115250305_115250307delinsGAA	GRCh37
NC_000001.9:g.115051828_115051830delinsGAA	NCBI36
NG_007572.1:g.14209_14211delinsTTC , LRG_92:g.14209_14211delinsTTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000369535.5:c.*408_*410delinsTTC MANE Select	ENSP00000358548.4:n.*408_*410delinsTTC
ENST00000369535.4:c.*408_*410delinsTTC	ENSP00000358548.4:n.*408_*410delinsTTC
NM_002524.4:c.*408_*410delinsTTC	NP_002515.1:n.*408_*410delinsTTC
NM_002524.5:c.*408_*410delinsTTC MANE Select	NP_002515.1:n.*408_*410delinsTTC