Canonical Allele Identifier: CA2340507963
Gene: RRAS HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49636594C= , CM000681.2:g.49636594C= GRCh38
NC_000019.9:g.50139851C= , CM000681.1:g.50139851C= GRCh37
NC_000019.8:g.54831663C= NCBI36
NG_042222.1:g.8550G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000246792.4:c.453+25G= MANE Select ENSP00000246792.2:n.453+25G=
ENST00000246792.3:c.453+25G= ENSP00000246792.2:n.453+25G=
ENST00000601532.1:n.593+25G=
NM_006270.3:c.453+25G= NP_006261.1:n.453+25G=
NM_006270.4:c.453+25G= NP_006261.1:n.453+25G=
NM_006270.5:c.453+25G= MANE Select NP_006261.1:n.453+25G=
Search 100 bp 5'
Search 100 bp 3'