Canonical Allele Identifier: CA2340507823
Gene: RRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49636310T= , CM000681.2:g.49636310T= GRCh38
NC_000019.9:g.50139567T= , CM000681.1:g.50139567T= GRCh37
NC_000019.8:g.54831379T= NCBI36
NG_042222.1:g.8834A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000246792.4:c.453+309A= MANE Select ENSP00000246792.2:n.453+309A=
ENST00000246792.3:c.453+309A= ENSP00000246792.2:n.453+309A=
ENST00000601532.1:n.593+309A=
NM_006270.3:c.453+309A= NP_006261.1:n.453+309A=
NM_006270.4:c.453+309A= NP_006261.1:n.453+309A=
NM_006270.5:c.453+309A= MANE Select NP_006261.1:n.453+309A=