Canonical Allele Identifier: CA1190284312
Gene: NRAS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114705275_114705276delinsTA , CM000663.2:g.114705275_114705276delinsTA GRCh38
NC_000001.10:g.115247896_115247897delinsTA , CM000663.1:g.115247896_115247897delinsTA GRCh37
NC_000001.9:g.115049419_115049420delinsTA NCBI36
NG_007572.1:g.16619_16620delinsTA , LRG_92:g.16619_16620delinsTA

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.*2818_*2819delinsTA MANE Select ENSP00000358548.4:n.*2818_*2819delinsTA
ENST00000369535.4:c.*2818_*2819delinsTA ENSP00000358548.4:n.*2818_*2819delinsTA
NM_002524.4:c.*2818_*2819delinsTA NP_002515.1:n.*2818_*2819delinsTA
NM_002524.5:c.*2818_*2819delinsTA MANE Select NP_002515.1:n.*2818_*2819delinsTA
Search 100 bp 5'
Search 100 bp 3'