Canonical Allele Identifier: CA406846231
Gene: RRAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49636657A>T , CM000681.2:g.49636657A>T GRCh38
NC_000019.9:g.50139914A>T , CM000681.1:g.50139914A>T GRCh37
NC_000019.8:g.54831726A>T NCBI36
NG_042222.1:g.8487T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000246792.4:c.415T>A MANE Select ENSP00000246792.2:p.Leu139Met
ENST00000246792.3:c.415T>A ENSP00000246792.2:p.Leu139Met
ENST00000601532.1:n.555T>A
NM_006270.3:c.415T>A NP_006261.1:p.Leu139Met
NM_006270.4:c.415T>A NP_006261.1:p.Leu139Met
NM_006270.5:c.415T>A MANE Select NP_006261.1:p.Leu139Met