Canonical Allele Identifier: CA379862797

Gene: RRAS2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.14358803C>T , CM000673.2:g.14358803C>T	GRCh38
NC_000011.9:g.14380349C>T , CM000673.1:g.14380349C>T	GRCh37
NC_000011.8:g.14336925C>T	NCBI36
NG_017058.1:g.10704G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_012250.6:c.68G>A MANE Select	NP_036382.2:p.Gly23Asp
ENST00000256196.9:c.68G>A MANE Select	ENSP00000256196.4:p.Gly23Asp
NM_001177314.1:c.3+5588G>A	NP_001170785.1:n.3+5588G>A
NM_001177314.2:c.3+5588G>A	NP_001170785.1:n.3+5588G>A
NM_012250.5:c.68G>A	NP_036382.2:p.Gly23Asp
ENST00000256196.8:c.68G>A	ENSP00000256196.4:p.Gly23Asp
ENST00000526717.1:c.68G>A	ENSP00000436887.1:p.Gly23Asp
ENST00000529237.5:c.-124+5588G>A	ENSP00000433230.1:n.-124+5588G>A
ENST00000532950.5:c.68G>A	ENSP00000436190.1:p.Gly23Asp
ENST00000537760.5:c.3+5588G>A	ENSP00000437547.1:n.3+5588G>A
ENST00000545643.5:c.65G>A	ENSP00000441722.2:p.Gly22Asp