Canonical Allele Identifier: CA2250667420

Gene: RAI1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17793808_17793830delinsAGCAGCAGCAGCAAGCCCTTCAG , CM000679.2:g.17793808_17793830delinsAGCAGCAGCAGCAAGCCCTTCAG	GRCh38
NC_000017.10:g.17697122_17697144delinsAGCAGCAGCAGCAAGCCCTTCAG , CM000679.1:g.17697122_17697144delinsAGCAGCAGCAGCAAGCCCTTCAG	GRCh37
NC_000017.9:g.17637847_17637869delinsAGCAGCAGCAGCAAGCCCTTCAG	NCBI36
NG_007101.2:g.117336_117358delinsAGCAGCAGCAGCAAGCCCTTCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000353383.6:c.860_882delinsAGCAGCAGCAGCAAGCCCTTCAG MANE Select	ENSP00000323074.4:p.Gln287=
ENST00000640861.1:c.794_816delinsAGCAGCAGCAGCAAGCCCTTCAG	ENSP00000491773.1:p.Gln265=
ENST00000353383.5:c.860_882delinsAGCAGCAGCAGCAAGCCCTTCAG	ENSP00000323074.4:p.Gln287=
ENST00000395774.1:c.860_882delinsAGCAGCAGCAGCAAGCCCTTCAG	ENSP00000379120.1:p.Gln287=
NM_030665.3:c.860_882delinsAGCAGCAGCAGCAAGCCCTTCAG	NP_109590.3:p.Gln287=
XM_017024025.1:c.860_882delinsAGCAGCAGCAGCAAGCCCTTCAG	XP_016879514.1:p.Gln287=
XM_017024026.1:c.860_882delinsAGCAGCAGCAGCAAGCCCTTCAG	XP_016879515.1:p.Gln287=
XM_017024027.1:c.860_882delinsAGCAGCAGCAGCAAGCCCTTCAG	XP_016879516.1:p.Gln287=
XM_017024028.2:c.860_882delinsAGCAGCAGCAGCAAGCCCTTCAG	XP_016879517.1:p.Gln287=
NM_030665.4:c.860_882delinsAGCAGCAGCAGCAAGCCCTTCAG MANE Select	NP_109590.3:p.Gln287=