Canonical Allele Identifier: CA1190289411

Gene: NRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114709438_114709443delinsAAAAAT , CM000663.2:g.114709438_114709443delinsAAAAAT	GRCh38
NC_000001.10:g.115252059_115252064delinsAAAAAT , CM000663.1:g.115252059_115252064delinsAAAAAT	GRCh37
NC_000001.9:g.115053582_115053587delinsAAAAAT	NCBI36
NG_007572.1:g.12452_12457delinsATTTTT , LRG_92:g.12452_12457delinsATTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.450+126_450+131delinsATTTTT MANE Select	ENSP00000358548.4:n.450+126_450+131delinsATTTTT
ENST00000369535.4:c.450+126_450+131delinsATTTTT	ENSP00000358548.4:n.450+126_450+131delinsATTTTT
NM_002524.4:c.450+126_450+131delinsATTTTT	NP_002515.1:n.450+126_450+131delinsATTTTT
NM_002524.5:c.450+126_450+131delinsATTTTT MANE Select	NP_002515.1:n.450+126_450+131delinsATTTTT