Canonical Allele Identifier: CA2340507962
Gene: RRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49636593T= , CM000681.2:g.49636593T= GRCh38
NC_000019.9:g.50139850T= , CM000681.1:g.50139850T= GRCh37
NC_000019.8:g.54831662T= NCBI36
NG_042222.1:g.8551A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000246792.4:c.453+26A= MANE Select ENSP00000246792.2:n.453+26A=
ENST00000246792.3:c.453+26A= ENSP00000246792.2:n.453+26A=
ENST00000601532.1:n.593+26A=
NM_006270.3:c.453+26A= NP_006261.1:n.453+26A=
NM_006270.4:c.453+26A= NP_006261.1:n.453+26A=
NM_006270.5:c.453+26A= MANE Select NP_006261.1:n.453+26A=