Canonical Allele Identifier: CA2250666539

Gene: RAI1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17793637G= , CM000679.2:g.17793637G=	GRCh38
NC_000017.10:g.17696951G= , CM000679.1:g.17696951G=	GRCh37
NC_000017.9:g.17637676G=	NCBI36
NG_007101.2:g.117165G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000353383.6:c.689G= MANE Select	ENSP00000323074.4:p.Gly230=
ENST00000640861.1:c.624G=	ENSP00000491773.1:p.Trp208=
ENST00000353383.5:c.689G=	ENSP00000323074.4:p.Gly230=
ENST00000395774.1:c.689G=	ENSP00000379120.1:p.Gly230=
NM_030665.3:c.689G=	NP_109590.3:p.Gly230=
XM_017024025.1:c.689G=	XP_016879514.1:p.Gly230=
XM_017024026.1:c.689G=	XP_016879515.1:p.Gly230=
XM_017024027.1:c.689G=	XP_016879516.1:p.Gly230=
XM_017024028.2:c.689G=	XP_016879517.1:p.Gly230=
NM_030665.4:c.689G= MANE Select	NP_109590.3:p.Gly230=