Canonical Allele Identifier: CA29039645
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs61652108
gnomAD v2: 1-115247749-T-TA
gnomAD v3: 1-114705128-T-TA
gnomAD v4: 1-114705128-T-TA
MyVariant Identifiers: chr1:g.115247750_115247751insA (hg19) chr1:g.115247749_115247750insA (hg19) chr1:g.114705129_114705130insA (hg38) chr1:g.114705128_114705129insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114705135dup , CM000663.2:g.114705135dup GRCh38
NC_000001.10:g.115247756dup , CM000663.1:g.115247756dup GRCh37
NC_000001.9:g.115049279dup NCBI36
NG_007572.1:g.16766dup , LRG_92:g.16766dup

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.*2965dup MANE Select ENSP00000358548.4:n.*2965dup
ENST00000369535.4:c.*2965dup ENSP00000358548.4:n.*2965dup
NM_002524.4:c.*2965dup NP_002515.1:n.*2965dup
NM_002524.5:c.*2965dup MANE Select NP_002515.1:n.*2965dup
Search 100 bp 5'
Search 100 bp 3'