Canonical Allele Identifier: CA1190289407

Gene: NRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114709435_114709450delinsAAAAAAAATAAAAAAT , CM000663.2:g.114709435_114709450delinsAAAAAAAATAAAAAAT	GRCh38
NC_000001.10:g.115252056_115252071delinsAAAAAAAATAAAAAAT , CM000663.1:g.115252056_115252071delinsAAAAAAAATAAAAAAT	GRCh37
NC_000001.9:g.115053579_115053594delinsAAAAAAAATAAAAAAT	NCBI36
NG_007572.1:g.12445_12460delinsATTTTTTATTTTTTTT , LRG_92:g.12445_12460delinsATTTTTTATTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.450+119_450+134delinsATTTTTTATTTTTTTT MANE Select	ENSP00000358548.4:n.450+119_450+134delinsATTTTTTATTTTTTTT
ENST00000369535.4:c.450+119_450+134delinsATTTTTTATTTTTTTT	ENSP00000358548.4:n.450+119_450+134delinsATTTTTTATTTTTTTT
NM_002524.4:c.450+119_450+134delinsATTTTTTATTTTTTTT	NP_002515.1:n.450+119_450+134delinsATTTTTTATTTTTTTT
NM_002524.5:c.450+119_450+134delinsATTTTTTATTTTTTTT MANE Select	NP_002515.1:n.450+119_450+134delinsATTTTTTATTTTTTTT