Canonical Allele Identifier: CA2299126109

Gene: RIT2

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.42857724G= , CM000680.2:g.42857724G=	GRCh38
NC_000018.9:g.40437689G= , CM000680.1:g.40437689G=	GRCh37
NC_000018.8:g.38691687G=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000326695.10:c.426+65848C= MANE Select	ENSP00000321805.4:n.426+65848C=
ENST00000650392.1:c.*56-12555C=	ENSP00000497708.1:n.*56-12555C=
ENST00000326695.9:c.426+65848C=	ENSP00000321805.4:n.426+65848C=
ENST00000589109.5:c.*28+62973C=	ENSP00000467217.1:n.*28+62973C=
ENST00000590910.1:c.488+65848C=	ENSP00000466620.1:n.488+65848C=
NM_001272077.1:c.*28+62973C=	NP_001259006.1:n.*28+62973C=
NM_002930.3:c.426+65848C=	NP_002921.1:n.426+65848C=
NM_002930.4:c.426+65848C= MANE Select	NP_002921.1:n.426+65848C=
NM_001272077.2:c.*28+62973C=	NP_001259006.1:n.*28+62973C=