Canonical Allele Identifier: CA2340507911
Gene: RRAS HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49636492G= , CM000681.2:g.49636492G= GRCh38
NC_000019.9:g.50139749G= , CM000681.1:g.50139749G= GRCh37
NC_000019.8:g.54831561G= NCBI36
NG_042222.1:g.8652C=

Transcript Alleles

HGVS Amino-acid change
ENST00000246792.4:c.453+127C= MANE Select ENSP00000246792.2:n.453+127C=
ENST00000246792.3:c.453+127C= ENSP00000246792.2:n.453+127C=
ENST00000601532.1:n.593+127C=
NM_006270.3:c.453+127C= NP_006261.1:n.453+127C=
NM_006270.4:c.453+127C= NP_006261.1:n.453+127C=
NM_006270.5:c.453+127C= MANE Select NP_006261.1:n.453+127C=
Search 100 bp 5'
Search 100 bp 3'