Canonical Allele Identifier: CA1190289584

Gene: NRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114709892_114709893delinsCA , CM000663.2:g.114709892_114709893delinsCA	GRCh38
NC_000001.10:g.115252513_115252514delinsCA , CM000663.1:g.115252513_115252514delinsCA	GRCh37
NC_000001.9:g.115054036_115054037delinsCA	NCBI36
NG_007572.1:g.12002_12003delinsTG , LRG_92:g.12002_12003delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.291-165_291-164delinsTG MANE Select	ENSP00000358548.4:n.291-165_291-164delinsTG
ENST00000369535.4:c.291-165_291-164delinsTG	ENSP00000358548.4:n.291-165_291-164delinsTG
NM_002524.4:c.291-165_291-164delinsTG	NP_002515.1:n.291-165_291-164delinsTG
NM_002524.5:c.291-165_291-164delinsTG MANE Select	NP_002515.1:n.291-165_291-164delinsTG