Canonical Allele Identifier: CA1190291305

Gene: NRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114713907_114713908delinsTT , CM000663.2:g.114713907_114713908delinsTT	GRCh38
NC_000001.10:g.115256528_115256529delinsTT , CM000663.1:g.115256528_115256529delinsTT	GRCh37
NC_000001.9:g.115058051_115058052delinsTT	NCBI36
NG_007572.1:g.7987_7988delinsAA , LRG_92:g.7987_7988delinsAA

Transcript Alleles

HGVS	Amino-acid change
ENST00000369535.5:c.182_183delinsAA MANE Select	ENSP00000358548.4:p.Gln61=
ENST00000369535.4:c.182_183delinsAA	ENSP00000358548.4:p.Gln61=
NM_002524.4:c.182_183delinsAA	NP_002515.1:p.Gln61=
NM_002524.5:c.182_183delinsAA MANE Select	NP_002515.1:p.Gln61=