Canonical Allele Identifier: CA2814696111
Gene: RRAS HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49636350G>A , CM000681.2:g.49636350G>A GRCh38
NC_000019.9:g.50139607G>A , CM000681.1:g.50139607G>A GRCh37
NC_000019.8:g.54831419G>A NCBI36
NG_042222.1:g.8794C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000246792.4:c.453+269C>T MANE Select ENSP00000246792.2:n.453+269C>T
ENST00000246792.3:c.453+269C>T ENSP00000246792.2:n.453+269C>T
ENST00000601532.1:n.593+269C>T
NM_006270.3:c.453+269C>T NP_006261.1:n.453+269C>T
NM_006270.4:c.453+269C>T NP_006261.1:n.453+269C>T
NM_006270.5:c.453+269C>T MANE Select NP_006261.1:n.453+269C>T
Search 100 bp 5'
Search 100 bp 3'