Canonical Allele Identifier: CA2299239264

Gene: RIT2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.43098355C= , CM000680.2:g.43098355C=	GRCh38
NC_000018.9:g.40678320C= , CM000680.1:g.40678320C=	GRCh37
NC_000018.8:g.38932318C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000326695.10:c.103+17062G= MANE Select	ENSP00000321805.4:n.103+17062G=
ENST00000650392.1:c.103+17062G=	ENSP00000497708.1:n.103+17062G=
ENST00000326695.9:c.103+17062G=	ENSP00000321805.4:n.103+17062G=
ENST00000589109.5:c.103+17062G=	ENSP00000467217.1:n.103+17062G=
ENST00000590910.1:c.103+17062G=	ENSP00000466620.1:n.103+17062G=
NM_001272077.1:c.103+17062G=	NP_001259006.1:n.103+17062G=
NM_002930.3:c.103+17062G=	NP_002921.1:n.103+17062G=
NM_002930.4:c.103+17062G= MANE Select	NP_002921.1:n.103+17062G=
NM_001272077.2:c.103+17062G=	NP_001259006.1:n.103+17062G=