Canonical Allele Identifier: CA2574035386
Gene: NRAS HGNC NCBI

Linked Data

gnomAD v4: 1-114713733-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114713733C>T , CM000663.2:g.114713733C>T GRCh38
NC_000001.10:g.115256354C>T , CM000663.1:g.115256354C>T GRCh37
NC_000001.9:g.115057877C>T NCBI36
NG_007572.1:g.8162G>A , LRG_92:g.8162G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.290+67G>A MANE Select ENSP00000358548.4:n.290+67G>A
ENST00000369535.4:c.290+67G>A ENSP00000358548.4:n.290+67G>A
NM_002524.4:c.290+67G>A NP_002515.1:n.290+67G>A
NM_002524.5:c.290+67G>A MANE Select NP_002515.1:n.290+67G>A
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