Canonical Allele Identifier: CA398546456

Gene: RAI1

Linked Data

• ClinVar Variation Id: 3019704
• ClinVar RCV Id: RCV003874815
• dbSNP Id: rs1252586358
• gnomAD v3: 17-17793851-A-T
• gnomAD v4: 17-17793851-A-T
• MyVariant Identifiers: chr17:g.17697165A>T (hg19) ; chr17:g.17793851A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17793851A>T , CM000679.2:g.17793851A>T	GRCh38
NC_000017.10:g.17697165A>T , CM000679.1:g.17697165A>T	GRCh37
NC_000017.9:g.17637890A>T	NCBI36
NG_007101.2:g.117379A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000353383.6:c.903A>T MANE Select	ENSP00000323074.4:p.Glu301Asp
ENST00000640861.1:c.837A>T	ENSP00000491773.1:p.Glu279Asp
ENST00000353383.5:c.903A>T	ENSP00000323074.4:p.Glu301Asp
ENST00000395774.1:c.903A>T	ENSP00000379120.1:p.Glu301Asp
NM_030665.3:c.903A>T	NP_109590.3:p.Glu301Asp
XM_017024025.1:c.903A>T	XP_016879514.1:p.Glu301Asp
XM_017024026.1:c.903A>T	XP_016879515.1:p.Glu301Asp
XM_017024027.1:c.903A>T	XP_016879516.1:p.Glu301Asp
XM_017024028.2:c.903A>T	XP_016879517.1:p.Glu301Asp
NM_030665.4:c.903A>T MANE Select	NP_109590.3:p.Glu301Asp