Canonical Allele Identifier: CA2647248594
Gene: NRAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114714010_114714011del , CM000663.2:g.114714010_114714011del GRCh38
NC_000001.10:g.115256631_115256632del , CM000663.1:g.115256631_115256632del GRCh37
NC_000001.9:g.115058154_115058155del NCBI36
NG_007572.1:g.7885_7886del , LRG_92:g.7885_7886del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.112-32_112-31del MANE Select ENSP00000358548.4:n.112-32_112-31del
ENST00000369535.4:c.112-32_112-31del ENSP00000358548.4:n.112-32_112-31del
NM_002524.4:c.112-32_112-31del NP_002515.1:n.112-32_112-31del
NM_002524.5:c.112-32_112-31del MANE Select NP_002515.1:n.112-32_112-31del