Canonical Allele Identifier: CA2250667137
Gene: RAI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.17793781_17793782delinsAG , CM000679.2:g.17793781_17793782delinsAG GRCh38
NC_000017.10:g.17697095_17697096delinsAG , CM000679.1:g.17697095_17697096delinsAG GRCh37
NC_000017.9:g.17637820_17637821delinsAG NCBI36
NG_007101.2:g.117309_117310delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000353383.6:c.833_834delinsAG MANE Select ENSP00000323074.4:p.Gln278=
ENST00000640861.1:c.767_768delinsAG ENSP00000491773.1:p.Gln256=
ENST00000353383.5:c.833_834delinsAG ENSP00000323074.4:p.Gln278=
ENST00000395774.1:c.833_834delinsAG ENSP00000379120.1:p.Gln278=
NM_030665.3:c.833_834delinsAG NP_109590.3:p.Gln278=
XM_017024025.1:c.833_834delinsAG XP_016879514.1:p.Gln278=
XM_017024026.1:c.833_834delinsAG XP_016879515.1:p.Gln278=
XM_017024027.1:c.833_834delinsAG XP_016879516.1:p.Gln278=
XM_017024028.2:c.833_834delinsAG XP_016879517.1:p.Gln278=
NM_030665.4:c.833_834delinsAG MANE Select NP_109590.3:p.Gln278=