Canonical Allele Identifier: CA2340507981

Gene: RRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49636627G= , CM000681.2:g.49636627G=	GRCh38
NC_000019.9:g.50139884G= , CM000681.1:g.50139884G=	GRCh37
NC_000019.8:g.54831696G=	NCBI36
NG_042222.1:g.8517C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000246792.4:c.445C= MANE Select	ENSP00000246792.2:p.Gln149=
ENST00000246792.3:c.445C=	ENSP00000246792.2:p.Gln149=
ENST00000601532.1:n.585C=
NM_006270.3:c.445C=	NP_006261.1:p.Gln149=
NM_006270.4:c.445C=	NP_006261.1:p.Gln149=
NM_006270.5:c.445C= MANE Select	NP_006261.1:p.Gln149=