Canonical Allele Identifier: CA2250666275
Gene: RAI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.17793556_17793557delinsTC , CM000679.2:g.17793556_17793557delinsTC GRCh38
NC_000017.10:g.17696870_17696871delinsTC , CM000679.1:g.17696870_17696871delinsTC GRCh37
NC_000017.9:g.17637595_17637596delinsTC NCBI36
NG_007101.2:g.117084_117085delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000353383.6:c.608_609delinsTC MANE Select ENSP00000323074.4:p.Phe203=
ENST00000640861.1:c.608_609delinsTC ENSP00000491773.1:p.Phe203=
ENST00000353383.5:c.608_609delinsTC ENSP00000323074.4:p.Phe203=
ENST00000395774.1:c.608_609delinsTC ENSP00000379120.1:p.Phe203=
NM_030665.3:c.608_609delinsTC NP_109590.3:p.Phe203=
XM_017024025.1:c.608_609delinsTC XP_016879514.1:p.Phe203=
XM_017024026.1:c.608_609delinsTC XP_016879515.1:p.Phe203=
XM_017024027.1:c.608_609delinsTC XP_016879516.1:p.Phe203=
XM_017024028.2:c.608_609delinsTC XP_016879517.1:p.Phe203=
NM_030665.4:c.608_609delinsTC MANE Select NP_109590.3:p.Phe203=