Canonical Allele Identifier: CA2340507787
Gene: RRAS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49636231C= , CM000681.2:g.49636231C= GRCh38
NC_000019.9:g.50139488C= , CM000681.1:g.50139488C= GRCh37
NC_000019.8:g.54831300C= NCBI36
NG_042222.1:g.8913G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000246792.4:c.454-379G= MANE Select ENSP00000246792.2:n.454-379G=
ENST00000246792.3:c.454-379G= ENSP00000246792.2:n.454-379G=
ENST00000601532.1:n.594-379G=
NM_006270.3:c.454-379G= NP_006261.1:n.454-379G=
NM_006270.4:c.454-379G= NP_006261.1:n.454-379G=
NM_006270.5:c.454-379G= MANE Select NP_006261.1:n.454-379G=
Search 100 bp 5'
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