Canonical Allele Identifier: CA341742621
Gene: NRAS HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.115258735T>G (hg19) chr1:g.114716114T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114716114T>G , CM000663.2:g.114716114T>G GRCh38
NC_000001.10:g.115258735T>G , CM000663.1:g.115258735T>G GRCh37
NC_000001.9:g.115060258T>G NCBI36
NG_007572.1:g.5781A>C , LRG_92:g.5781A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.47A>C MANE Select ENSP00000358548.4:p.Lys16Thr
ENST00000369535.4:c.47A>C ENSP00000358548.4:p.Lys16Thr
NM_002524.4:c.47A>C NP_002515.1:p.Lys16Thr
NM_002524.5:c.47A>C MANE Select NP_002515.1:p.Lys16Thr
Search 100 bp 5'
Search 100 bp 3'