Canonical Allele Identifier: CA1190292183
Gene: NRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114716110_114716111delinsGC , CM000663.2:g.114716110_114716111delinsGC GRCh38
NC_000001.10:g.115258731_115258732delinsGC , CM000663.1:g.115258731_115258732delinsGC GRCh37
NC_000001.9:g.115060254_115060255delinsGC NCBI36
NG_007572.1:g.5784_5785delinsGC , LRG_92:g.5784_5785delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.50_51delinsGC MANE Select ENSP00000358548.4:p.Ser17=
ENST00000369535.4:c.50_51delinsGC ENSP00000358548.4:p.Ser17=
NM_002524.4:c.50_51delinsGC NP_002515.1:p.Ser17=
NM_002524.5:c.50_51delinsGC MANE Select NP_002515.1:p.Ser17=