Canonical Allele Identifier: CA2603521482
Gene: NRAS HGNC NCBI

Linked Data

gnomAD v3: 1-114705988-CCAGT-C
gnomAD v4: 1-114705988-CCAGT-C
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114705991_114705994del , CM000663.2:g.114705991_114705994del GRCh38
NC_000001.10:g.115248612_115248615del , CM000663.1:g.115248612_115248615del GRCh37
NC_000001.9:g.115050135_115050138del NCBI36
NG_007572.1:g.15903_15906del , LRG_92:g.15903_15906del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*2102_*2105del MANE Select ENSP00000358548.4:n.*2102_*2105del
ENST00000369535.4:c.*2102_*2105del ENSP00000358548.4:n.*2102_*2105del
NM_002524.4:c.*2102_*2105del NP_002515.1:n.*2102_*2105del
NM_002524.5:c.*2102_*2105del MANE Select NP_002515.1:n.*2102_*2105del
Search 100 bp 5'
Search 100 bp 3'