Canonical Allele Identifier: CA1190284292
Gene: NRAS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114705227A= , CM000663.2:g.114705227A= GRCh38
NC_000001.10:g.115247848A= , CM000663.1:g.115247848A= GRCh37
NC_000001.9:g.115049371A= NCBI36
NG_007572.1:g.16668T= , LRG_92:g.16668T=

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.*2867T= MANE Select ENSP00000358548.4:n.*2867T=
ENST00000369535.4:c.*2867T= ENSP00000358548.4:n.*2867T=
NM_002524.4:c.*2867T= NP_002515.1:n.*2867T=
NM_002524.5:c.*2867T= MANE Select NP_002515.1:n.*2867T=
Search 100 bp 5'
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