Canonical Allele Identifier: CA885812188
Gene: NRAS HGNC NCBI

Linked Data

dbSNP Id: rs1414191541
gnomAD v3: 1-114714170-TA-T
gnomAD v4: 1-114714170-TA-T
MyVariant Identifiers: chr1:g.115256792del (hg19) chr1:g.114714171del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114714174del , CM000663.2:g.114714174del GRCh38
NC_000001.10:g.115256795del , CM000663.1:g.115256795del GRCh37
NC_000001.9:g.115058318del NCBI36
NG_007572.1:g.7724del , LRG_92:g.7724del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.112-193del MANE Select ENSP00000358548.4:n.112-193del
ENST00000369535.4:c.112-193del ENSP00000358548.4:n.112-193del
NM_002524.4:c.112-193del NP_002515.1:n.112-193del
NM_002524.5:c.112-193del MANE Select NP_002515.1:n.112-193del
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