Canonical Allele Identifier: CA341742656
Gene: NRAS HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.115258742C>A (hg19) chr1:g.114716121C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114716121C>A , CM000663.2:g.114716121C>A GRCh38
NC_000001.10:g.115258742C>A , CM000663.1:g.115258742C>A GRCh37
NC_000001.9:g.115060265C>A NCBI36
NG_007572.1:g.5774G>T , LRG_92:g.5774G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.40G>T MANE Select ENSP00000358548.4:p.Val14Phe
ENST00000369535.4:c.40G>T ENSP00000358548.4:p.Val14Phe
NM_002524.4:c.40G>T NP_002515.1:p.Val14Phe
NM_002524.5:c.40G>T MANE Select NP_002515.1:p.Val14Phe
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Search 100 bp 3'