Canonical Allele Identifier: CA2735964997
Gene: RRAS HGNC NCBI

Linked Data

dbSNP Id: rs2122418249

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49636352del , CM000681.2:g.49636352del GRCh38
NC_000019.9:g.50139609del , CM000681.1:g.50139609del GRCh37
NC_000019.8:g.54831421del NCBI36
NG_042222.1:g.8793del

Transcript Alleles

HGVS Amino-acid Change
ENST00000246792.4:c.453+268del MANE Select ENSP00000246792.2:n.453+268del
ENST00000246792.3:c.453+268del ENSP00000246792.2:n.453+268del
ENST00000601532.1:n.593+268del
NM_006270.3:c.453+268del NP_006261.1:n.453+268del
NM_006270.4:c.453+268del NP_006261.1:n.453+268del
NM_006270.5:c.453+268del MANE Select NP_006261.1:n.453+268del