Canonical Allele Identifier: CA2586409080
Gene: RRAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49636583_49636584del , CM000681.2:g.49636583_49636584del GRCh38
NC_000019.9:g.50139840_50139841del , CM000681.1:g.50139840_50139841del GRCh37
NC_000019.8:g.54831652_54831653del NCBI36
NG_042222.1:g.8560_8561del

Transcript Alleles

HGVS Amino-acid Change
ENST00000246792.4:c.453+35_453+36del MANE Select ENSP00000246792.2:n.453+35_453+36del
ENST00000246792.3:c.453+35_453+36del ENSP00000246792.2:n.453+35_453+36del
ENST00000601532.1:n.593+35_593+36del
NM_006270.3:c.453+35_453+36del NP_006261.1:n.453+35_453+36del
NM_006270.4:c.453+35_453+36del NP_006261.1:n.453+35_453+36del
NM_006270.5:c.453+35_453+36del MANE Select NP_006261.1:n.453+35_453+36del