Canonical Allele Identifier: CA2250667178

Gene: RAI1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17793784_17793786delinsAGC , CM000679.2:g.17793784_17793786delinsAGC	GRCh38
NC_000017.10:g.17697098_17697100delinsAGC , CM000679.1:g.17697098_17697100delinsAGC	GRCh37
NC_000017.9:g.17637823_17637825delinsAGC	NCBI36
NG_007101.2:g.117312_117314delinsAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000353383.6:c.836_838delinsAGC MANE Select	ENSP00000323074.4:p.Gln279=
ENST00000640861.1:c.770_772delinsAGC	ENSP00000491773.1:p.Gln257=
ENST00000353383.5:c.836_838delinsAGC	ENSP00000323074.4:p.Gln279=
ENST00000395774.1:c.836_838delinsAGC	ENSP00000379120.1:p.Gln279=
NM_030665.3:c.836_838delinsAGC	NP_109590.3:p.Gln279=
XM_017024025.1:c.836_838delinsAGC	XP_016879514.1:p.Gln279=
XM_017024026.1:c.836_838delinsAGC	XP_016879515.1:p.Gln279=
XM_017024027.1:c.836_838delinsAGC	XP_016879516.1:p.Gln279=
XM_017024028.2:c.836_838delinsAGC	XP_016879517.1:p.Gln279=
NM_030665.4:c.836_838delinsAGC MANE Select	NP_109590.3:p.Gln279=