Canonical Allele Identifier: CA645537995
Gene: NRAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713909_114713910insGGAAGC , CM000663.2:g.114713909_114713910insGGAAGC GRCh38
NC_000001.10:g.115256530_115256531insGGAAGC , CM000663.1:g.115256530_115256531insGGAAGC GRCh37
NC_000001.9:g.115058053_115058054insGGAAGC NCBI36
NG_007572.1:g.7985_7986insGCTTCC , LRG_92:g.7985_7986insGCTTCC

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.180_181insGCTTCC MANE Select ENSP00000358548.4:p.Gly60_Gln61insAlaSer
ENST00000369535.4:c.180_181insGCTTCC ENSP00000358548.4:p.Gly60_Gln61insAlaSer
NM_002524.4:c.180_181insGCTTCC NP_002515.1:p.Gly60_Gln61insAlaSer
NM_002524.5:c.180_181insGCTTCC MANE Select NP_002515.1:p.Gly60_Gln61insAlaSer