Canonical Allele Identifier: CA1190289459

Gene: NRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114709527_114709528delinsCT , CM000663.2:g.114709527_114709528delinsCT	GRCh38
NC_000001.10:g.115252148_115252149delinsCT , CM000663.1:g.115252148_115252149delinsCT	GRCh37
NC_000001.9:g.115053671_115053672delinsCT	NCBI36
NG_007572.1:g.12367_12368delinsAG , LRG_92:g.12367_12368delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.450+41_450+42delinsAG MANE Select	ENSP00000358548.4:n.450+41_450+42delinsAG
ENST00000369535.4:c.450+41_450+42delinsAG	ENSP00000358548.4:n.450+41_450+42delinsAG
NM_002524.4:c.450+41_450+42delinsAG	NP_002515.1:n.450+41_450+42delinsAG
NM_002524.5:c.450+41_450+42delinsAG MANE Select	NP_002515.1:n.450+41_450+42delinsAG