Canonical Allele Identifier: CA885826083
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1221136640
gnomAD v3: 1-114705170-CT-C
gnomAD v4: 1-114705170-CT-C
MyVariant Identifiers: chr1:g.115247792del (hg19) chr1:g.114705171del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114705173del , CM000663.2:g.114705173del GRCh38
NC_000001.10:g.115247794del , CM000663.1:g.115247794del GRCh37
NC_000001.9:g.115049317del NCBI36
NG_007572.1:g.16724del , LRG_92:g.16724del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*2923del MANE Select ENSP00000358548.4:n.*2923del
ENST00000369535.4:c.*2923del ENSP00000358548.4:n.*2923del
NM_002524.4:c.*2923del NP_002515.1:n.*2923del
NM_002524.5:c.*2923del MANE Select NP_002515.1:n.*2923del
Search 100 bp 5'
Search 100 bp 3'