Canonical Allele Identifier: CA2814696110
Gene: RRAS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49636335A>T , CM000681.2:g.49636335A>T GRCh38
NC_000019.9:g.50139592A>T , CM000681.1:g.50139592A>T GRCh37
NC_000019.8:g.54831404A>T NCBI36
NG_042222.1:g.8809T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000246792.4:c.453+284T>A MANE Select ENSP00000246792.2:n.453+284T>A
ENST00000246792.3:c.453+284T>A ENSP00000246792.2:n.453+284T>A
ENST00000601532.1:n.593+284T>A
NM_006270.3:c.453+284T>A NP_006261.1:n.453+284T>A
NM_006270.4:c.453+284T>A NP_006261.1:n.453+284T>A
NM_006270.5:c.453+284T>A MANE Select NP_006261.1:n.453+284T>A
Search 100 bp 5'
Search 100 bp 3'