Canonical Allele Identifier: CA2647253267
Gene: NRAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709539_114709540del , CM000663.2:g.114709539_114709540del GRCh38
NC_000001.10:g.115252160_115252161del , CM000663.1:g.115252160_115252161del GRCh37
NC_000001.9:g.115053683_115053684del NCBI36
NG_007572.1:g.12357_12358del , LRG_92:g.12357_12358del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.450+31_450+32del MANE Select ENSP00000358548.4:n.450+31_450+32del
ENST00000369535.4:c.450+31_450+32del ENSP00000358548.4:n.450+31_450+32del
NM_002524.4:c.450+31_450+32del NP_002515.1:n.450+31_450+32del
NM_002524.5:c.450+31_450+32del MANE Select NP_002515.1:n.450+31_450+32del