Canonical Allele Identifier: CA379862795
Community Standard Title: NM_012250.6(RRAS2):c.68G>T (p.Gly23Val)
Gene: RRAS2 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
NM_012250.6:c.68G>T MANE Select NP_036382.2:p.Gly23Val
ENST00000256196.9:c.68G>T MANE Select ENSP00000256196.4:p.Gly23Val
NM_001177314.1:c.3+5588G>T NP_001170785.1:n.3+5588G>T
NM_001177314.2:c.3+5588G>T NP_001170785.1:n.3+5588G>T
NM_012250.5:c.68G>T NP_036382.2:p.Gly23Val
ENST00000256196.8:c.68G>T ENSP00000256196.4:p.Gly23Val
ENST00000526717.1:c.68G>T ENSP00000436887.1:p.Gly23Val
ENST00000529237.5:c.-124+5588G>T ENSP00000433230.1:n.-124+5588G>T
ENST00000532950.5:c.68G>T ENSP00000436190.1:p.Gly23Val
ENST00000537760.5:c.3+5588G>T ENSP00000437547.1:n.3+5588G>T
ENST00000545643.5:c.65G>T ENSP00000441722.2:p.Gly22Val