Canonical Allele Identifier: CA726622927

Gene: RAI1

Linked Data

• dbSNP Id: rs1396218186
• MyVariant Identifiers: chr17:g.17697091_17697093del (hg19) ; chr17:g.17793777_17793779del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17793777_17793779del , CM000679.2:g.17793777_17793779del	GRCh38
NC_000017.10:g.17697091_17697093del , CM000679.1:g.17697091_17697093del	GRCh37
NC_000017.9:g.17637816_17637818del	NCBI36
NG_007101.2:g.117305_117307del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000353383.6:c.829_831del MANE Select	ENSP00000323074.4:p.Asp277del
ENST00000640861.1:c.763_765del	ENSP00000491773.1:p.Asp255del
ENST00000353383.5:c.829_831del	ENSP00000323074.4:p.Asp277del
ENST00000395774.1:c.829_831del	ENSP00000379120.1:p.Asp277del
NM_030665.3:c.829_831del	NP_109590.3:p.Asp277del
XM_017024025.1:c.829_831del	XP_016879514.1:p.Asp277del
XM_017024026.1:c.829_831del	XP_016879515.1:p.Asp277del
XM_017024027.1:c.829_831del	XP_016879516.1:p.Asp277del
XM_017024028.2:c.829_831del	XP_016879517.1:p.Asp277del
NM_030665.4:c.829_831del MANE Select	NP_109590.3:p.Asp277del