Canonical Allele Identifier: CA2647248946
Gene: NRAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114716013_114716014del , CM000663.2:g.114716013_114716014del GRCh38
NC_000001.10:g.115258634_115258635del , CM000663.1:g.115258634_115258635del GRCh37
NC_000001.9:g.115060157_115060158del NCBI36
NG_007572.1:g.5885_5886del , LRG_92:g.5885_5886del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.111+40_111+41del MANE Select ENSP00000358548.4:n.111+40_111+41del
ENST00000369535.4:c.111+40_111+41del ENSP00000358548.4:n.111+40_111+41del
NM_002524.4:c.111+40_111+41del NP_002515.1:n.111+40_111+41del
NM_002524.5:c.111+40_111+41del MANE Select NP_002515.1:n.111+40_111+41del