Canonical Allele Identifier: CA1190289394

Gene: NRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114709419_114709421delinsAGT , CM000663.2:g.114709419_114709421delinsAGT	GRCh38
NC_000001.10:g.115252040_115252042delinsAGT , CM000663.1:g.115252040_115252042delinsAGT	GRCh37
NC_000001.9:g.115053563_115053565delinsAGT	NCBI36
NG_007572.1:g.12474_12476delinsACT , LRG_92:g.12474_12476delinsACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.450+148_450+150delinsACT MANE Select	ENSP00000358548.4:n.450+148_450+150delinsACT
ENST00000369535.4:c.450+148_450+150delinsACT	ENSP00000358548.4:n.450+148_450+150delinsACT
NM_002524.4:c.450+148_450+150delinsACT	NP_002515.1:n.450+148_450+150delinsACT
NM_002524.5:c.450+148_450+150delinsACT MANE Select	NP_002515.1:n.450+148_450+150delinsACT