Canonical Allele Identifier: CA2735964802
Gene: RRAS HGNC NCBI

Linked Data

dbSNP Id: rs2122418196

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49636335del , CM000681.2:g.49636335del GRCh38
NC_000019.9:g.50139592del , CM000681.1:g.50139592del GRCh37
NC_000019.8:g.54831404del NCBI36
NG_042222.1:g.8810del

Transcript Alleles

HGVS Amino-acid Change
ENST00000246792.4:c.453+285del MANE Select ENSP00000246792.2:n.453+285del
ENST00000246792.3:c.453+285del ENSP00000246792.2:n.453+285del
ENST00000601532.1:n.593+285del
NM_006270.3:c.453+285del NP_006261.1:n.453+285del
NM_006270.4:c.453+285del NP_006261.1:n.453+285del
NM_006270.5:c.453+285del MANE Select NP_006261.1:n.453+285del