Canonical Allele Identifier: CA1190289391

Gene: NRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114709411_114709415delinsGAAGA , CM000663.2:g.114709411_114709415delinsGAAGA	GRCh38
NC_000001.10:g.115252032_115252036delinsGAAGA , CM000663.1:g.115252032_115252036delinsGAAGA	GRCh37
NC_000001.9:g.115053555_115053559delinsGAAGA	NCBI36
NG_007572.1:g.12480_12484delinsTCTTC , LRG_92:g.12480_12484delinsTCTTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.450+154_450+158delinsTCTTC MANE Select	ENSP00000358548.4:n.450+154_450+158delinsTCTTC
ENST00000369535.4:c.450+154_450+158delinsTCTTC	ENSP00000358548.4:n.450+154_450+158delinsTCTTC
NM_002524.4:c.450+154_450+158delinsTCTTC	NP_002515.1:n.450+154_450+158delinsTCTTC
NM_002524.5:c.450+154_450+158delinsTCTTC MANE Select	NP_002515.1:n.450+154_450+158delinsTCTTC