Canonical Allele Identifier: CA1190284859
Gene: NRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114705952T= , CM000663.2:g.114705952T= GRCh38
NC_000001.10:g.115248573T= , CM000663.1:g.115248573T= GRCh37
NC_000001.9:g.115050096T= NCBI36
NG_007572.1:g.15943A= , LRG_92:g.15943A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*2142A= MANE Select ENSP00000358548.4:n.*2142A=
ENST00000369535.4:c.*2142A= ENSP00000358548.4:n.*2142A=
NM_002524.4:c.*2142A= NP_002515.1:n.*2142A=
NM_002524.5:c.*2142A= MANE Select NP_002515.1:n.*2142A=