Canonical Allele Identifier: CA2647250227
Gene: NRAS HGNC NCBI

Linked Data

gnomAD v4: 1-114705926-TA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114705928del , CM000663.2:g.114705928del GRCh38
NC_000001.10:g.115248549del , CM000663.1:g.115248549del GRCh37
NC_000001.9:g.115050072del NCBI36
NG_007572.1:g.15968del , LRG_92:g.15968del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*2167del MANE Select ENSP00000358548.4:n.*2167del
ENST00000369535.4:c.*2167del ENSP00000358548.4:n.*2167del
NM_002524.4:c.*2167del NP_002515.1:n.*2167del
NM_002524.5:c.*2167del MANE Select NP_002515.1:n.*2167del
Search 100 bp 5'
Search 100 bp 3'