Canonical Allele Identifier: CA2636388231

Gene: RAI1

Linked Data

• gnomAD v4: 17-17793788-G-GCAA

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17793790_17793791insACA , CM000679.2:g.17793790_17793791insACA	GRCh38
NC_000017.10:g.17697104_17697105insACA , CM000679.1:g.17697104_17697105insACA	GRCh37
NC_000017.9:g.17637829_17637830insACA	NCBI36
NG_007101.2:g.117318_117319insACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000353383.6:c.842_843insACA MANE Select	ENSP00000323074.4:p.Gln281_Gln282insGln
ENST00000640861.1:c.776_777insACA	ENSP00000491773.1:p.Gln259_Gln260insGln
ENST00000353383.5:c.842_843insACA	ENSP00000323074.4:p.Gln281_Gln282insGln
ENST00000395774.1:c.842_843insACA	ENSP00000379120.1:p.Gln281_Gln282insGln
NM_030665.3:c.842_843insACA	NP_109590.3:p.Gln281_Gln282insGln
XM_017024025.1:c.842_843insACA	XP_016879514.1:p.Gln281_Gln282insGln
XM_017024026.1:c.842_843insACA	XP_016879515.1:p.Gln281_Gln282insGln
XM_017024027.1:c.842_843insACA	XP_016879516.1:p.Gln281_Gln282insGln
XM_017024028.2:c.842_843insACA	XP_016879517.1:p.Gln281_Gln282insGln
NM_030665.4:c.842_843insACA MANE Select	NP_109590.3:p.Gln281_Gln282insGln