Canonical Allele Identifier: CA525408049
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1319871433
gnomAD v2: 1-115247857-CTAAAA-C
gnomAD v3: 1-114705236-CTAAAA-C
gnomAD v4: 1-114705236-CTAAAA-C
MyVariant Identifiers: chr1:g.115247858_115247862del (hg19) chr1:g.114705237_114705241del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114705239_114705243del , CM000663.2:g.114705239_114705243del GRCh38
NC_000001.10:g.115247860_115247864del , CM000663.1:g.115247860_115247864del GRCh37
NC_000001.9:g.115049383_115049387del NCBI36
NG_007572.1:g.16654_16658del , LRG_92:g.16654_16658del

Transcript Alleles

HGVS Amino-acid change
ENST00000369535.5:c.*2853_*2857del MANE Select ENSP00000358548.4:n.*2853_*2857del
ENST00000369535.4:c.*2853_*2857del ENSP00000358548.4:n.*2853_*2857del
NM_002524.4:c.*2853_*2857del NP_002515.1:n.*2853_*2857del
NM_002524.5:c.*2853_*2857del MANE Select NP_002515.1:n.*2853_*2857del
Search 100 bp 5'
Search 100 bp 3'