Canonical Allele Identifier: CA13528580

Gene: RRAS2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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