Canonical Allele Identifier: CA2340040798

Gene: RASIP1

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.48725015T= , CM000681.2:g.48725015T=	GRCh38
NC_000019.9:g.49228272T= , CM000681.1:g.49228272T=	GRCh37
NC_000019.8:g.53920084T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_017805.3:c.2128-55A= MANE Select	NP_060275.2:n.2128-55A=
ENST00000222145.9:c.2128-55A= MANE Select	ENSP00000222145.3:n.2128-55A=
NM_017805.2:c.2128-55A=	NP_060275.2:n.2128-55A=
ENST00000222145.8:c.2128-55A=	ENSP00000222145.3:n.2128-55A=
ENST00000599291.1:c.416-55A=
ENST00000601530.1:n.567A=
ENST00000621604.4:c.2125-55A=	ENSP00000479419.1:n.2125-55A=
XM_011527053.1:c.2128-55A=	XP_011525355.1:n.2128-55A=
XM_011527053.2:c.2431-55A=	XP_011525355.2:n.2431-55A=
XM_011527054.1:c.2128-55A=	XP_011525356.1:n.2128-55A=
XM_011527055.1:c.1834-55A=	XP_011525357.1:n.1834-55A=
XM_017026914.1:c.2431-55A=	XP_016882403.1:n.2431-55A=
XM_017026915.1:c.2137-55A=	XP_016882404.1:n.2137-55A=
XM_024451566.1:c.2431-55A=	XP_024307334.1:n.2431-55A=
XM_024451567.1:c.2137-55A=	XP_024307335.1:n.2137-55A=
XR_001753712.1:n.2341-55A=
XR_935837.1:n.2321-55A=