Canonical Allele Identifier: CA1190284777
Gene: NRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114705861G= , CM000663.2:g.114705861G= GRCh38
NC_000001.10:g.115248482G= , CM000663.1:g.115248482G= GRCh37
NC_000001.9:g.115050005G= NCBI36
NG_007572.1:g.16034C= , LRG_92:g.16034C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*2233C= MANE Select ENSP00000358548.4:n.*2233C=
ENST00000369535.4:c.*2233C= ENSP00000358548.4:n.*2233C=
NM_002524.4:c.*2233C= NP_002515.1:n.*2233C=
NM_002524.5:c.*2233C= MANE Select NP_002515.1:n.*2233C=