Canonical Allele Identifier: CA341739773
Gene: NRAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709718T>G , CM000663.2:g.114709718T>G GRCh38
NC_000001.10:g.115252339T>G , CM000663.1:g.115252339T>G GRCh37
NC_000001.9:g.115053862T>G NCBI36
NG_007572.1:g.12177A>C , LRG_92:g.12177A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.301A>C MANE Select ENSP00000358548.4:p.Lys101Gln
ENST00000369535.4:c.301A>C ENSP00000358548.4:p.Lys101Gln
NM_002524.4:c.301A>C NP_002515.1:p.Lys101Gln
NM_002524.5:c.301A>C MANE Select NP_002515.1:p.Lys101Gln