Canonical Allele Identifier: CA2636388229

Gene: RAI1

Linked Data

• gnomAD v4: 17-17793779-C-CCGG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17793780_17793781insGGC , CM000679.2:g.17793780_17793781insGGC	GRCh38
NC_000017.10:g.17697094_17697095insGGC , CM000679.1:g.17697094_17697095insGGC	GRCh37
NC_000017.9:g.17637819_17637820insGGC	NCBI36
NG_007101.2:g.117308_117309insGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000353383.6:c.832_833insGGC MANE Select	ENSP00000323074.4:p.Asp277_Gln278insArg
ENST00000640861.1:c.766_767insGGC	ENSP00000491773.1:p.Asp255_Gln256insArg
ENST00000353383.5:c.832_833insGGC	ENSP00000323074.4:p.Asp277_Gln278insArg
ENST00000395774.1:c.832_833insGGC	ENSP00000379120.1:p.Asp277_Gln278insArg
NM_030665.3:c.832_833insGGC	NP_109590.3:p.Asp277_Gln278insArg
XM_017024025.1:c.832_833insGGC	XP_016879514.1:p.Asp277_Gln278insArg
XM_017024026.1:c.832_833insGGC	XP_016879515.1:p.Asp277_Gln278insArg
XM_017024027.1:c.832_833insGGC	XP_016879516.1:p.Asp277_Gln278insArg
XM_017024028.2:c.832_833insGGC	XP_016879517.1:p.Asp277_Gln278insArg
NM_030665.4:c.832_833insGGC MANE Select	NP_109590.3:p.Asp277_Gln278insArg