Canonical Allele Identifier: CA2647251664
Gene: NRAS HGNC NCBI

Linked Data

gnomAD v4: 1-114708114-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114708114A>C , CM000663.2:g.114708114A>C GRCh38
NC_000001.10:g.115250735A>C , CM000663.1:g.115250735A>C GRCh37
NC_000001.9:g.115052258A>C NCBI36
NG_007572.1:g.13781T>G , LRG_92:g.13781T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.*43+40T>G MANE Select ENSP00000358548.4:n.*43+40T>G
ENST00000369535.4:c.*43+40T>G ENSP00000358548.4:n.*43+40T>G
NM_002524.4:c.*43+40T>G NP_002515.1:n.*43+40T>G
NM_002524.5:c.*43+40T>G MANE Select NP_002515.1:n.*43+40T>G
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