Canonical Allele Identifier: CA2814696107
Gene: RRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49636215G>A , CM000681.2:g.49636215G>A GRCh38
NC_000019.9:g.50139472G>A , CM000681.1:g.50139472G>A GRCh37
NC_000019.8:g.54831284G>A NCBI36
NG_042222.1:g.8929C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000246792.4:c.454-363C>T MANE Select ENSP00000246792.2:n.454-363C>T
ENST00000246792.3:c.454-363C>T ENSP00000246792.2:n.454-363C>T
ENST00000601532.1:n.594-363C>T
NM_006270.3:c.454-363C>T NP_006261.1:n.454-363C>T
NM_006270.4:c.454-363C>T NP_006261.1:n.454-363C>T
NM_006270.5:c.454-363C>T MANE Select NP_006261.1:n.454-363C>T