Canonical Allele Identifier: CA2559829018
Gene: RRAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49636211_49636215del , CM000681.2:g.49636211_49636215del GRCh38
NC_000019.9:g.50139468_50139472del , CM000681.1:g.50139468_50139472del GRCh37
NC_000019.8:g.54831280_54831284del NCBI36
NG_042222.1:g.8929_8933del

Transcript Alleles

HGVS Amino-acid Change
ENST00000246792.4:c.454-363_454-359del MANE Select ENSP00000246792.2:n.454-363_454-359del
ENST00000246792.3:c.454-363_454-359del ENSP00000246792.2:n.454-363_454-359del
ENST00000601532.1:n.594-363_594-359del
NM_006270.3:c.454-363_454-359del NP_006261.1:n.454-363_454-359del
NM_006270.4:c.454-363_454-359del NP_006261.1:n.454-363_454-359del
NM_006270.5:c.454-363_454-359del MANE Select NP_006261.1:n.454-363_454-359del