Canonical Allele Identifier: CA1953727400

Gene: RRAS2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.14338889G= , CM000673.2:g.14338889G=	GRCh38
NC_000011.9:g.14360435G= , CM000673.1:g.14360435G=	GRCh37
NC_000011.8:g.14317011G=	NCBI36
NG_017058.1:g.30618C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000256196.9:c.108+19874C= MANE Select	ENSP00000256196.4:n.108+19874C=
ENST00000256196.8:c.108+19874C=	ENSP00000256196.4:n.108+19874C=
ENST00000526063.5:c.-124+19368C=	ENSP00000434104.1:n.-124+19368C=
ENST00000526717.1:c.108+19874C=	ENSP00000436887.1:n.108+19874C=
ENST00000529237.5:c.-124+25502C=	ENSP00000433230.1:n.-124+25502C=
ENST00000531807.5:c.51+2921C=	ENSP00000435453.1:n.51+2921C=
ENST00000532814.5:c.-124+19349C=	ENSP00000431954.1:n.-124+19349C=
ENST00000532950.5:c.*48+17797C=	ENSP00000436190.1:n.*48+17797C=
ENST00000534746.5:c.-124+15524C=	ENSP00000437083.1:n.-124+15524C=
ENST00000537760.5:c.3+25502C=	ENSP00000437547.1:n.3+25502C=
ENST00000545643.5:c.105+19874C=	ENSP00000441722.2:n.105+19874C=
NM_001102669.2:c.-124+19368C=	NP_001096139.1:n.-124+19368C=
NM_001177314.1:c.3+25502C=	NP_001170785.1:n.3+25502C=
NM_001177315.1:c.-124+19349C=	NP_001170786.1:n.-124+19349C=
NM_012250.5:c.108+19874C=	NP_036382.2:n.108+19874C=
NM_012250.6:c.108+19874C= MANE Select	NP_036382.2:n.108+19874C=
NM_001177314.2:c.3+25502C=	NP_001170785.1:n.3+25502C=