Canonical Allele Identifier: CA1190289472

Gene: NRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114709553_114709554delinsGA , CM000663.2:g.114709553_114709554delinsGA	GRCh38
NC_000001.10:g.115252174_115252175delinsGA , CM000663.1:g.115252174_115252175delinsGA	GRCh37
NC_000001.9:g.115053697_115053698delinsGA	NCBI36
NG_007572.1:g.12341_12342delinsTC , LRG_92:g.12341_12342delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.450+15_450+16delinsTC MANE Select	ENSP00000358548.4:n.450+15_450+16delinsTC
ENST00000369535.4:c.450+15_450+16delinsTC	ENSP00000358548.4:n.450+15_450+16delinsTC
NM_002524.4:c.450+15_450+16delinsTC	NP_002515.1:n.450+15_450+16delinsTC
NM_002524.5:c.450+15_450+16delinsTC MANE Select	NP_002515.1:n.450+15_450+16delinsTC