Canonical Allele Identifier: CA2340507958

Gene: RRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49636585A= , CM000681.2:g.49636585A=	GRCh38
NC_000019.9:g.50139842A= , CM000681.1:g.50139842A=	GRCh37
NC_000019.8:g.54831654A=	NCBI36
NG_042222.1:g.8559T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000246792.4:c.453+34T= MANE Select	ENSP00000246792.2:n.453+34T=
ENST00000246792.3:c.453+34T=	ENSP00000246792.2:n.453+34T=
ENST00000601532.1:n.593+34T=
NM_006270.3:c.453+34T=	NP_006261.1:n.453+34T=
NM_006270.4:c.453+34T=	NP_006261.1:n.453+34T=
NM_006270.5:c.453+34T= MANE Select	NP_006261.1:n.453+34T=