Canonical Allele Identifier: CA2696723123

Gene: NRAS

Linked Data

• dbSNP Id: rs2101736319

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114705943_114705947del , CM000663.2:g.114705943_114705947del	GRCh38
NC_000001.10:g.115248564_115248568del , CM000663.1:g.115248564_115248568del	GRCh37
NC_000001.9:g.115050087_115050091del	NCBI36
NG_007572.1:g.15949_15953del , LRG_92:g.15949_15953del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.*2148_*2152del MANE Select	ENSP00000358548.4:n.*2148_*2152del
ENST00000369535.4:c.*2148_*2152del	ENSP00000358548.4:n.*2148_*2152del
NM_002524.4:c.*2148_*2152del	NP_002515.1:n.*2148_*2152del
NM_002524.5:c.*2148_*2152del MANE Select	NP_002515.1:n.*2148_*2152del