Canonical Allele Identifier: CA885828595
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1444647333
MyVariant Identifiers: chr1:g.115252666_115252667insC (hg19) chr1:g.114710045_114710046insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114710047dup , CM000663.2:g.114710047dup GRCh38
NC_000001.10:g.115252668dup , CM000663.1:g.115252668dup GRCh37
NC_000001.9:g.115054191dup NCBI36
NG_007572.1:g.11849dup , LRG_92:g.11849dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.291-318dup MANE Select ENSP00000358548.4:n.291-318dup
ENST00000369535.4:c.291-318dup ENSP00000358548.4:n.291-318dup
NM_002524.4:c.291-318dup NP_002515.1:n.291-318dup
NM_002524.5:c.291-318dup MANE Select NP_002515.1:n.291-318dup
Search 100 bp 5'
Search 100 bp 3'