Canonical Allele Identifier: CA2250666437

Gene: RAI1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17793611C= , CM000679.2:g.17793611C=	GRCh38
NC_000017.10:g.17696925C= , CM000679.1:g.17696925C=	GRCh37
NC_000017.9:g.17637650C=	NCBI36
NG_007101.2:g.117139C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000353383.6:c.663C= MANE Select	ENSP00000323074.4:p.Thr221=
ENST00000640861.1:c.617-19C=	ENSP00000491773.1:n.617-19C=
ENST00000353383.5:c.663C=	ENSP00000323074.4:p.Thr221=
ENST00000395774.1:c.663C=	ENSP00000379120.1:p.Thr221=
NM_030665.3:c.663C=	NP_109590.3:p.Thr221=
XM_017024025.1:c.663C=	XP_016879514.1:p.Thr221=
XM_017024026.1:c.663C=	XP_016879515.1:p.Thr221=
XM_017024027.1:c.663C=	XP_016879516.1:p.Thr221=
XM_017024028.2:c.663C=	XP_016879517.1:p.Thr221=
NM_030665.4:c.663C= MANE Select	NP_109590.3:p.Thr221=