Canonical Allele Identifier: CA2647250764
Gene: NRAS HGNC NCBI

Linked Data

gnomAD v4: 1-114707048-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114707048G>T , CM000663.2:g.114707048G>T GRCh38
NC_000001.10:g.115249669G>T , CM000663.1:g.115249669G>T GRCh37
NC_000001.9:g.115051192G>T NCBI36
NG_007572.1:g.14847C>A , LRG_92:g.14847C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.*1046C>A MANE Select ENSP00000358548.4:n.*1046C>A
ENST00000369535.4:c.*1046C>A ENSP00000358548.4:n.*1046C>A
NM_002524.4:c.*1046C>A NP_002515.1:n.*1046C>A
NM_002524.5:c.*1046C>A MANE Select NP_002515.1:n.*1046C>A
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