Canonical Allele Identifier: CA5894276
Community Standard Title: NM_012250.6(RRAS2):c.409-16A>T
Gene: RRAS2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.14281736T>A , CM000673.2:g.14281736T>A GRCh38
NC_000011.9:g.14303282T>A , CM000673.1:g.14303282T>A GRCh37
NC_000011.8:g.14259858T>A NCBI36
NG_017058.1:g.87771A>T

Transcript Alleles

HGVS Amino-acid Change
NM_012250.6:c.409-16A>T MANE Select NP_036382.2:n.409-16A>T
ENST00000256196.9:c.409-16A>T MANE Select ENSP00000256196.4:n.409-16A>T
NM_001102669.2:c.178-16A>T NP_001096139.1:n.178-16A>T
NM_001177314.1:c.304-16A>T NP_001170785.1:n.304-16A>T
NM_001177314.2:c.304-16A>T NP_001170785.1:n.304-16A>T
NM_001177315.1:c.178-16A>T NP_001170786.1:n.178-16A>T
NM_012250.5:c.409-16A>T NP_036382.2:n.409-16A>T
ENST00000256196.8:c.409-16A>T ENSP00000256196.4:n.409-16A>T
ENST00000414023.6:c.178-16A>T ENSP00000403282.2:n.178-16A>T
ENST00000526063.5:c.178-16A>T ENSP00000434104.1:n.178-16A>T
ENST00000529237.5:c.178-16A>T ENSP00000433230.1:n.178-16A>T
ENST00000531421.5:c.178-16A>T ENSP00000432559.1:n.178-16A>T
ENST00000531807.5:c.352-16A>T ENSP00000435453.1:n.352-16A>T
ENST00000532814.5:c.178-16A>T ENSP00000431954.1:n.178-16A>T
ENST00000532950.5:c.*349-16A>T ENSP00000436190.1:n.*349-16A>T
ENST00000534746.5:c.178-16A>T ENSP00000437083.1:n.178-16A>T
ENST00000537760.5:c.304-16A>T ENSP00000437547.1:n.304-16A>T
ENST00000545643.5:c.406-16A>T ENSP00000441722.2:n.406-16A>T
XM_017017363.1:c.343-16A>T XP_016872852.1:n.343-16A>T
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