Canonical Allele Identifier: CA406846281
Gene: RRAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49636665G>A , CM000681.2:g.49636665G>A GRCh38
NC_000019.9:g.50139922G>A , CM000681.1:g.50139922G>A GRCh37
NC_000019.8:g.54831734G>A NCBI36
NG_042222.1:g.8479C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000246792.4:c.407C>T MANE Select ENSP00000246792.2:p.Pro136Leu
ENST00000246792.3:c.407C>T ENSP00000246792.2:p.Pro136Leu
ENST00000601532.1:n.547C>T
NM_006270.3:c.407C>T NP_006261.1:p.Pro136Leu
NM_006270.4:c.407C>T NP_006261.1:p.Pro136Leu
NM_006270.5:c.407C>T MANE Select NP_006261.1:p.Pro136Leu