Canonical Allele Identifier: CA2250667446

Gene: RAI1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17793815_17793821delinsGCAGCAA , CM000679.2:g.17793815_17793821delinsGCAGCAA	GRCh38
NC_000017.10:g.17697129_17697135delinsGCAGCAA , CM000679.1:g.17697129_17697135delinsGCAGCAA	GRCh37
NC_000017.9:g.17637854_17637860delinsGCAGCAA	NCBI36
NG_007101.2:g.117343_117349delinsGCAGCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000353383.6:c.867_873delinsGCAGCAA MANE Select	ENSP00000323074.4:p.Gln289=
ENST00000640861.1:c.801_807delinsGCAGCAA	ENSP00000491773.1:p.Gln267=
ENST00000353383.5:c.867_873delinsGCAGCAA	ENSP00000323074.4:p.Gln289=
ENST00000395774.1:c.867_873delinsGCAGCAA	ENSP00000379120.1:p.Gln289=
NM_030665.3:c.867_873delinsGCAGCAA	NP_109590.3:p.Gln289=
XM_017024025.1:c.867_873delinsGCAGCAA	XP_016879514.1:p.Gln289=
XM_017024026.1:c.867_873delinsGCAGCAA	XP_016879515.1:p.Gln289=
XM_017024027.1:c.867_873delinsGCAGCAA	XP_016879516.1:p.Gln289=
XM_017024028.2:c.867_873delinsGCAGCAA	XP_016879517.1:p.Gln289=
NM_030665.4:c.867_873delinsGCAGCAA MANE Select	NP_109590.3:p.Gln289=