Canonical Allele Identifier: CA2340507912
Gene: RRAS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49636495G= , CM000681.2:g.49636495G= GRCh38
NC_000019.9:g.50139752G= , CM000681.1:g.50139752G= GRCh37
NC_000019.8:g.54831564G= NCBI36
NG_042222.1:g.8649C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000246792.4:c.453+124C= MANE Select ENSP00000246792.2:n.453+124C=
ENST00000246792.3:c.453+124C= ENSP00000246792.2:n.453+124C=
ENST00000601532.1:n.593+124C=
NM_006270.3:c.453+124C= NP_006261.1:n.453+124C=
NM_006270.4:c.453+124C= NP_006261.1:n.453+124C=
NM_006270.5:c.453+124C= MANE Select NP_006261.1:n.453+124C=
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