Canonical Allele Identifier: CA2250666558

Gene: RAI1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17793645_17793646delinsGC , CM000679.2:g.17793645_17793646delinsGC	GRCh38
NC_000017.10:g.17696959_17696960delinsGC , CM000679.1:g.17696959_17696960delinsGC	GRCh37
NC_000017.9:g.17637684_17637685delinsGC	NCBI36
NG_007101.2:g.117173_117174delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000353383.6:c.697_698delinsGC MANE Select	ENSP00000323074.4:p.Ala233=
ENST00000640861.1:c.632_633delinsGC	ENSP00000491773.1:p.Gly211=
ENST00000353383.5:c.697_698delinsGC	ENSP00000323074.4:p.Ala233=
ENST00000395774.1:c.697_698delinsGC	ENSP00000379120.1:p.Ala233=
NM_030665.3:c.697_698delinsGC	NP_109590.3:p.Ala233=
XM_017024025.1:c.697_698delinsGC	XP_016879514.1:p.Ala233=
XM_017024026.1:c.697_698delinsGC	XP_016879515.1:p.Ala233=
XM_017024027.1:c.697_698delinsGC	XP_016879516.1:p.Ala233=
XM_017024028.2:c.697_698delinsGC	XP_016879517.1:p.Ala233=
NM_030665.4:c.697_698delinsGC MANE Select	NP_109590.3:p.Ala233=