Canonical Allele Identifier: CA2647250180
Gene: NRAS HGNC NCBI

Linked Data

gnomAD v4: 1-114705798-TA-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.114705800del , CM000663.2:g.114705800del GRCh38
NC_000001.10:g.115248421del , CM000663.1:g.115248421del GRCh37
NC_000001.9:g.115049944del NCBI36
NG_007572.1:g.16096del , LRG_92:g.16096del

Transcript Alleles

HGVS Amino-acid Change
ENST00000369535.5:c.*2295del MANE Select ENSP00000358548.4:n.*2295del
ENST00000369535.4:c.*2295del ENSP00000358548.4:n.*2295del
NM_002524.4:c.*2295del NP_002515.1:n.*2295del
NM_002524.5:c.*2295del MANE Select NP_002515.1:n.*2295del
Search 100 bp 5'
Search 100 bp 3'