Canonical Allele Identifier: CA2340507853

Gene: RRAS

Linked Data

• dbSNP Id: rs1224001494

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49636380del , CM000681.2:g.49636380del	GRCh38
NC_000019.9:g.50139637del , CM000681.1:g.50139637del	GRCh37
NC_000019.8:g.54831449del	NCBI36
NG_042222.1:g.8769del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000246792.4:c.453+244del MANE Select	ENSP00000246792.2:n.453+244del
ENST00000246792.3:c.453+244del	ENSP00000246792.2:n.453+244del
ENST00000601532.1:n.593+244del
NM_006270.3:c.453+244del	NP_006261.1:n.453+244del
NM_006270.4:c.453+244del	NP_006261.1:n.453+244del
NM_006270.5:c.453+244del MANE Select	NP_006261.1:n.453+244del