Canonical Allele Identifier: CA726622472

Gene: RAI1

Linked Data

• dbSNP Id: rs1486844659
• MyVariant Identifiers: chr17:g.17696912_17696914del (hg19) ; chr17:g.17793598_17793600del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17793600_17793602del , CM000679.2:g.17793600_17793602del	GRCh38
NC_000017.10:g.17696914_17696916del , CM000679.1:g.17696914_17696916del	GRCh37
NC_000017.9:g.17637639_17637641del	NCBI36
NG_007101.2:g.117128_117130del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000353383.6:c.652_654del MANE Select	ENSP00000323074.4:p.Thr218del
ENST00000640861.1:c.617-30_617-28del	ENSP00000491773.1:n.617-30_617-28del
ENST00000353383.5:c.652_654del	ENSP00000323074.4:p.Thr218del
ENST00000395774.1:c.652_654del	ENSP00000379120.1:p.Thr218del
NM_030665.3:c.652_654del	NP_109590.3:p.Thr218del
XM_017024025.1:c.652_654del	XP_016879514.1:p.Thr218del
XM_017024026.1:c.652_654del	XP_016879515.1:p.Thr218del
XM_017024027.1:c.652_654del	XP_016879516.1:p.Thr218del
XM_017024028.2:c.652_654del	XP_016879517.1:p.Thr218del
NM_030665.4:c.652_654del MANE Select	NP_109590.3:p.Thr218del