Canonical Allele Identifier: CA2579753936
Gene: NRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713905_114713908delinsA , CM000663.2:g.114713905_114713908delinsA GRCh38
NC_000001.10:g.115256526_115256529delinsA , CM000663.1:g.115256526_115256529delinsA GRCh37
NC_000001.9:g.115058049_115058052delinsA NCBI36
NG_007572.1:g.7987_7990delinsT , LRG_92:g.7987_7990delinsT

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.182_185delinsT MANE Select ENSP00000358548.4:p.Gln61_Glu62delinsLeu
ENST00000369535.4:c.182_185delinsT ENSP00000358548.4:p.Gln61_Glu62delinsLeu
NM_002524.4:c.182_185delinsT NP_002515.1:p.Gln61_Glu62delinsLeu
NM_002524.5:c.182_185delinsT MANE Select NP_002515.1:p.Gln61_Glu62delinsLeu