Canonical Allele Identifier: CA625314488

Gene: RAI1

Linked Data

• dbSNP Id: rs1263846130
• gnomAD v2: 17-17697110-AGC-A
• MyVariant Identifiers: chr17:g.17697111_17697112del (hg19) ; chr17:g.17793797_17793798del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17793797_17793798del , CM000679.2:g.17793797_17793798del	GRCh38
NC_000017.10:g.17697111_17697112del , CM000679.1:g.17697111_17697112del	GRCh37
NC_000017.9:g.17637836_17637837del	NCBI36
NG_007101.2:g.117325_117326del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000353383.6:c.849_850del MANE Select	ENSP00000323074.4:p.Gln284AlafsTer?
ENST00000640861.1:c.783_784del	ENSP00000491773.1:p.Gln262AlafsTer?
ENST00000353383.5:c.849_850del	ENSP00000323074.4:p.Gln284AlafsTer?
ENST00000395774.1:c.849_850del	ENSP00000379120.1:p.Gln284AlafsTer?
NM_030665.3:c.849_850del	NP_109590.3:p.Gln284AlafsTer?
XM_017024025.1:c.849_850del	XP_016879514.1:p.Gln284AlafsTer?
XM_017024026.1:c.849_850del	XP_016879515.1:p.Gln284AlafsTer?
XM_017024027.1:c.849_850del	XP_016879516.1:p.Gln284AlafsTer?
XM_017024028.2:c.849_850del	XP_016879517.1:p.Gln284AlafsTer?
NM_030665.4:c.849_850del MANE Select	NP_109590.3:p.Gln284AlafsTer?