Canonical Allele Identifier: CA2340507797
Gene: RRAS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49636255C= , CM000681.2:g.49636255C= GRCh38
NC_000019.9:g.50139512C= , CM000681.1:g.50139512C= GRCh37
NC_000019.8:g.54831324C= NCBI36
NG_042222.1:g.8889G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000246792.4:c.453+364G= MANE Select ENSP00000246792.2:n.453+364G=
ENST00000246792.3:c.453+364G= ENSP00000246792.2:n.453+364G=
ENST00000601532.1:n.593+364G=
NM_006270.3:c.453+364G= NP_006261.1:n.453+364G=
NM_006270.4:c.453+364G= NP_006261.1:n.453+364G=
NM_006270.5:c.453+364G= MANE Select NP_006261.1:n.453+364G=
Search 100 bp 5'
Search 100 bp 3'