Canonical Allele Identifier: CA498423169
Gene: RAI1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.17697168C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.17793854C>A , CM000679.2:g.17793854C>A GRCh38
NC_000017.10:g.17697168C>A , CM000679.1:g.17697168C>A GRCh37
NC_000017.9:g.17637893C>A NCBI36
NG_007101.2:g.117382C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000353383.6:c.906C>A MANE Select ENSP00000323074.4:p.Thr302=
ENST00000640861.1:c.840C>A ENSP00000491773.1:p.Thr280=
ENST00000353383.5:c.906C>A ENSP00000323074.4:p.Thr302=
ENST00000395774.1:c.906C>A ENSP00000379120.1:p.Thr302=
NM_030665.3:c.906C>A NP_109590.3:p.Thr302=
XM_017024025.1:c.906C>A XP_016879514.1:p.Thr302=
XM_017024026.1:c.906C>A XP_016879515.1:p.Thr302=
XM_017024027.1:c.906C>A XP_016879516.1:p.Thr302=
XM_017024028.2:c.906C>A XP_016879517.1:p.Thr302=
NM_030665.4:c.906C>A MANE Select NP_109590.3:p.Thr302=
Search 100 bp 5'
Search 100 bp 3'