Canonical Allele Identifier: CA1190285488
Gene: NRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114706841C= , CM000663.2:g.114706841C= GRCh38
NC_000001.10:g.115249462C= , CM000663.1:g.115249462C= GRCh37
NC_000001.9:g.115050985C= NCBI36
NG_007572.1:g.15054G= , LRG_92:g.15054G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*1253G= MANE Select ENSP00000358548.4:n.*1253G=
ENST00000369535.4:c.*1253G= ENSP00000358548.4:n.*1253G=
NM_002524.4:c.*1253G= NP_002515.1:n.*1253G=
NM_002524.5:c.*1253G= MANE Select NP_002515.1:n.*1253G=