Canonical Allele Identifier: CA1005998569
Gene: NRAS HGNC NCBI

Linked Data

gnomAD v3: 1-114709967-C-A
gnomAD v4: 1-114709967-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114709967C>A , CM000663.2:g.114709967C>A GRCh38
NC_000001.10:g.115252588C>A , CM000663.1:g.115252588C>A GRCh37
NC_000001.9:g.115054111C>A NCBI36
NG_007572.1:g.11928G>T , LRG_92:g.11928G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.291-239G>T MANE Select ENSP00000358548.4:n.291-239G>T
ENST00000369535.4:c.291-239G>T ENSP00000358548.4:n.291-239G>T
NM_002524.4:c.291-239G>T NP_002515.1:n.291-239G>T
NM_002524.5:c.291-239G>T MANE Select NP_002515.1:n.291-239G>T
Search 100 bp 5'
Search 100 bp 3'