Canonical Allele Identifier: CA498422880

Gene: RAI1

Linked Data

• MyVariant Identifiers: chr17:g.17696892T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17793578T>C , CM000679.2:g.17793578T>C	GRCh38
NC_000017.10:g.17696892T>C , CM000679.1:g.17696892T>C	GRCh37
NC_000017.9:g.17637617T>C	NCBI36
NG_007101.2:g.117106T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000353383.6:c.630T>C MANE Select	ENSP00000323074.4:p.Pro210=
ENST00000640861.1:c.616+14T>C	ENSP00000491773.1:n.616+14T>C
ENST00000353383.5:c.630T>C	ENSP00000323074.4:p.Pro210=
ENST00000395774.1:c.630T>C	ENSP00000379120.1:p.Pro210=
NM_030665.3:c.630T>C	NP_109590.3:p.Pro210=
XM_017024025.1:c.630T>C	XP_016879514.1:p.Pro210=
XM_017024026.1:c.630T>C	XP_016879515.1:p.Pro210=
XM_017024027.1:c.630T>C	XP_016879516.1:p.Pro210=
XM_017024028.2:c.630T>C	XP_016879517.1:p.Pro210=
NM_030665.4:c.630T>C MANE Select	NP_109590.3:p.Pro210=