Canonical Allele Identifier: CA2340507799
Gene: RRAS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.49636272G= , CM000681.2:g.49636272G= GRCh38
NC_000019.9:g.50139529G= , CM000681.1:g.50139529G= GRCh37
NC_000019.8:g.54831341G= NCBI36
NG_042222.1:g.8872C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000246792.4:c.453+347C= MANE Select ENSP00000246792.2:n.453+347C=
ENST00000246792.3:c.453+347C= ENSP00000246792.2:n.453+347C=
ENST00000601532.1:n.593+347C=
NM_006270.3:c.453+347C= NP_006261.1:n.453+347C=
NM_006270.4:c.453+347C= NP_006261.1:n.453+347C=
NM_006270.5:c.453+347C= MANE Select NP_006261.1:n.453+347C=
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