Canonical Allele Identifier: CA2544426307

Gene: RRAS

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49636389C>A , CM000681.2:g.49636389C>A	GRCh38
NC_000019.9:g.50139646C>A , CM000681.1:g.50139646C>A	GRCh37
NC_000019.8:g.54831458C>A	NCBI36
NG_042222.1:g.8755G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000246792.4:c.453+230G>T MANE Select	ENSP00000246792.2:n.453+230G>T
ENST00000246792.3:c.453+230G>T	ENSP00000246792.2:n.453+230G>T
ENST00000601532.1:n.593+230G>T
NM_006270.3:c.453+230G>T	NP_006261.1:n.453+230G>T
NM_006270.4:c.453+230G>T	NP_006261.1:n.453+230G>T
NM_006270.5:c.453+230G>T MANE Select	NP_006261.1:n.453+230G>T