Canonical Allele Identifier: CA2340507780
Gene: RRAS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49636220G= , CM000681.2:g.49636220G= GRCh38
NC_000019.9:g.50139477G= , CM000681.1:g.50139477G= GRCh37
NC_000019.8:g.54831289G= NCBI36
NG_042222.1:g.8924C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000246792.4:c.454-368C= MANE Select ENSP00000246792.2:n.454-368C=
ENST00000246792.3:c.454-368C= ENSP00000246792.2:n.454-368C=
ENST00000601532.1:n.594-368C=
NM_006270.3:c.454-368C= NP_006261.1:n.454-368C=
NM_006270.4:c.454-368C= NP_006261.1:n.454-368C=
NM_006270.5:c.454-368C= MANE Select NP_006261.1:n.454-368C=
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