Canonical Allele Identifier: CA508130447

Gene: RRAS

Linked Data

• MyVariant Identifiers: chr19:g.50139891C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.49636634C>T , CM000681.2:g.49636634C>T	GRCh38
NC_000019.9:g.50139891C>T , CM000681.1:g.50139891C>T	GRCh37
NC_000019.8:g.54831703C>T	NCBI36
NG_042222.1:g.8510G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000246792.4:c.438G>A MANE Select	ENSP00000246792.2:p.Leu146=
ENST00000246792.3:c.438G>A	ENSP00000246792.2:p.Leu146=
ENST00000601532.1:n.578G>A
NM_006270.3:c.438G>A	NP_006261.1:p.Leu146=
NM_006270.4:c.438G>A	NP_006261.1:p.Leu146=
NM_006270.5:c.438G>A MANE Select	NP_006261.1:p.Leu146=