Canonical Allele Identifier: CA2696723211
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs2101736333
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114705964del , CM000663.2:g.114705964del GRCh38
NC_000001.10:g.115248585del , CM000663.1:g.115248585del GRCh37
NC_000001.9:g.115050108del NCBI36
NG_007572.1:g.15931del , LRG_92:g.15931del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*2130del MANE Select ENSP00000358548.4:n.*2130del
ENST00000369535.4:c.*2130del ENSP00000358548.4:n.*2130del
NM_002524.4:c.*2130del NP_002515.1:n.*2130del
NM_002524.5:c.*2130del MANE Select NP_002515.1:n.*2130del
Search 100 bp 5'
Search 100 bp 3'