Canonical Allele Identifier: CA406846372

Gene: RRAS

Linked Data

• MyVariant Identifiers: chr19:g.50139931T>A (hg19) ; chr19:g.49636674T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49636674T>A , CM000681.2:g.49636674T>A	GRCh38
NC_000019.9:g.50139931T>A , CM000681.1:g.50139931T>A	GRCh37
NC_000019.8:g.54831743T>A	NCBI36
NG_042222.1:g.8470A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000246792.4:c.398A>T MANE Select	ENSP00000246792.2:p.Asp133Val
ENST00000246792.3:c.398A>T	ENSP00000246792.2:p.Asp133Val
ENST00000601532.1:n.538A>T
NM_006270.3:c.398A>T	NP_006261.1:p.Asp133Val
NM_006270.4:c.398A>T	NP_006261.1:p.Asp133Val
NM_006270.5:c.398A>T MANE Select	NP_006261.1:p.Asp133Val