Canonical Allele Identifier: CA2636388230

Gene: RAI1

Linked Data

• gnomAD v4: 17-17793782-G-GCAT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17793784_17793785insTCA , CM000679.2:g.17793784_17793785insTCA	GRCh38
NC_000017.10:g.17697098_17697099insTCA , CM000679.1:g.17697098_17697099insTCA	GRCh37
NC_000017.9:g.17637823_17637824insTCA	NCBI36
NG_007101.2:g.117312_117313insTCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000353383.6:c.836_837insTCA MANE Select	ENSP00000323074.4:p.Gln278_Gln279insHis
ENST00000640861.1:c.770_771insTCA	ENSP00000491773.1:p.Gln256_Gln257insHis
ENST00000353383.5:c.836_837insTCA	ENSP00000323074.4:p.Gln278_Gln279insHis
ENST00000395774.1:c.836_837insTCA	ENSP00000379120.1:p.Gln278_Gln279insHis
NM_030665.3:c.836_837insTCA	NP_109590.3:p.Gln278_Gln279insHis
XM_017024025.1:c.836_837insTCA	XP_016879514.1:p.Gln278_Gln279insHis
XM_017024026.1:c.836_837insTCA	XP_016879515.1:p.Gln278_Gln279insHis
XM_017024027.1:c.836_837insTCA	XP_016879516.1:p.Gln278_Gln279insHis
XM_017024028.2:c.836_837insTCA	XP_016879517.1:p.Gln278_Gln279insHis
NM_030665.4:c.836_837insTCA MANE Select	NP_109590.3:p.Gln278_Gln279insHis