Canonical Allele Identifier: CA1190289424

Gene: NRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114709456_114709464delinsAATAAAAAT , CM000663.2:g.114709456_114709464delinsAATAAAAAT	GRCh38
NC_000001.10:g.115252077_115252085delinsAATAAAAAT , CM000663.1:g.115252077_115252085delinsAATAAAAAT	GRCh37
NC_000001.9:g.115053600_115053608delinsAATAAAAAT	NCBI36
NG_007572.1:g.12431_12439delinsATTTTTATT , LRG_92:g.12431_12439delinsATTTTTATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.450+105_450+113delinsATTTTTATT MANE Select	ENSP00000358548.4:n.450+105_450+113delinsATTTTTATT
ENST00000369535.4:c.450+105_450+113delinsATTTTTATT	ENSP00000358548.4:n.450+105_450+113delinsATTTTTATT
NM_002524.4:c.450+105_450+113delinsATTTTTATT	NP_002515.1:n.450+105_450+113delinsATTTTTATT
NM_002524.5:c.450+105_450+113delinsATTTTTATT MANE Select	NP_002515.1:n.450+105_450+113delinsATTTTTATT