Canonical Allele Identifier: CA2576917182
Gene: RRAS HGNC NCBI

Linked Data

gnomAD v4: 19-49636593-TC-T
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49636597del , CM000681.2:g.49636597del GRCh38
NC_000019.9:g.50139854del , CM000681.1:g.50139854del GRCh37
NC_000019.8:g.54831666del NCBI36
NG_042222.1:g.8550del

Transcript Alleles

HGVS Amino-acid Change
ENST00000246792.4:c.453+25del MANE Select ENSP00000246792.2:n.453+25del
ENST00000246792.3:c.453+25del ENSP00000246792.2:n.453+25del
ENST00000601532.1:n.593+25del
NM_006270.3:c.453+25del NP_006261.1:n.453+25del
NM_006270.4:c.453+25del NP_006261.1:n.453+25del
NM_006270.5:c.453+25del MANE Select NP_006261.1:n.453+25del
Search 100 bp 5'
Search 100 bp 3'