Canonical Allele Identifier: CA5894328

Gene: RRAS2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.14294851C>T , CM000673.2:g.14294851C>T	GRCh38
NC_000011.9:g.14316397C>T , CM000673.1:g.14316397C>T	GRCh37
NC_000011.8:g.14272973C>T	NCBI36
NG_017058.1:g.74656G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_012250.6:c.208G>A MANE Select	NP_036382.2:p.Ala70Thr
ENST00000256196.9:c.208G>A MANE Select	ENSP00000256196.4:p.Ala70Thr
NM_001102669.2:c.-24G>A	NP_001096139.1:n.-24G>A
NM_001177314.1:c.103G>A	NP_001170785.1:p.Ala35Thr
NM_001177314.2:c.103G>A	NP_001170785.1:p.Ala35Thr
NM_001177315.1:c.-24G>A	NP_001170786.1:n.-24G>A
NM_012250.5:c.208G>A	NP_036382.2:p.Ala70Thr
ENST00000256196.8:c.208G>A	ENSP00000256196.4:p.Ala70Thr
ENST00000414023.6:c.-24G>A	ENSP00000403282.2:n.-24G>A
ENST00000526063.5:c.-24G>A	ENSP00000434104.1:n.-24G>A
ENST00000526717.1:c.*160G>A	ENSP00000436887.1:n.*160G>A
ENST00000529237.5:c.-24G>A	ENSP00000433230.1:n.-24G>A
ENST00000531421.5:c.-24G>A	ENSP00000432559.1:n.-24G>A
ENST00000531807.5:c.151G>A	ENSP00000435453.1:p.Ala51Thr
ENST00000532814.5:c.-24G>A	ENSP00000431954.1:n.-24G>A
ENST00000532950.5:c.*148G>A	ENSP00000436190.1:n.*148G>A
ENST00000534746.5:c.-24G>A	ENSP00000437083.1:n.-24G>A
ENST00000537760.5:c.103G>A	ENSP00000437547.1:p.Ala35Thr
ENST00000545643.5:c.205G>A	ENSP00000441722.2:p.Ala69Thr
XM_017017363.1:c.142G>A	XP_016872852.1:p.Ala48Thr