Canonical Allele Identifier: CA2340507836
Gene: RRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49636339A= , CM000681.2:g.49636339A= GRCh38
NC_000019.9:g.50139596A= , CM000681.1:g.50139596A= GRCh37
NC_000019.8:g.54831408A= NCBI36
NG_042222.1:g.8805T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000246792.4:c.453+280T= MANE Select ENSP00000246792.2:n.453+280T=
ENST00000246792.3:c.453+280T= ENSP00000246792.2:n.453+280T=
ENST00000601532.1:n.593+280T=
NM_006270.3:c.453+280T= NP_006261.1:n.453+280T=
NM_006270.4:c.453+280T= NP_006261.1:n.453+280T=
NM_006270.5:c.453+280T= MANE Select NP_006261.1:n.453+280T=