Canonical Allele Identifier: CA1140536313

Gene: NRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114709434_114709442delinsAAAAAAAAA , CM000663.2:g.114709434_114709442delinsAAAAAAAAA	GRCh38
NC_000001.10:g.115252055_115252063delinsAAAAAAAAA , CM000663.1:g.115252055_115252063delinsAAAAAAAAA	GRCh37
NC_000001.9:g.115053578_115053586delinsAAAAAAAAA	NCBI36
NG_007572.1:g.12453_12461delinsTTTTTTTTT , LRG_92:g.12453_12461delinsTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.450+127_450+135delinsTTTTTTTTT MANE Select	ENSP00000358548.4:n.450+127_450+135delinsTTTTTTTTT
ENST00000369535.4:c.450+127_450+135delinsTTTTTTTTT	ENSP00000358548.4:n.450+127_450+135delinsTTTTTTTTT
NM_002524.4:c.450+127_450+135delinsTTTTTTTTT	NP_002515.1:n.450+127_450+135delinsTTTTTTTTT
NM_002524.5:c.450+127_450+135delinsTTTTTTTTT MANE Select	NP_002515.1:n.450+127_450+135delinsTTTTTTTTT