Canonical Allele Identifier: CA498422658

Gene: RAI1

Linked Data

• dbSNP Id: rs2032109421
• MyVariant Identifiers: chr17:g.17696976T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17793662T>C , CM000679.2:g.17793662T>C	GRCh38
NC_000017.10:g.17696976T>C , CM000679.1:g.17696976T>C	GRCh37
NC_000017.9:g.17637701T>C	NCBI36
NG_007101.2:g.117190T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000353383.6:c.714T>C MANE Select	ENSP00000323074.4:p.Ser238=
ENST00000640861.1:c.648T>C	ENSP00000491773.1:p.Ser216=
ENST00000353383.5:c.714T>C	ENSP00000323074.4:p.Ser238=
ENST00000395774.1:c.714T>C	ENSP00000379120.1:p.Ser238=
NM_030665.3:c.714T>C	NP_109590.3:p.Ser238=
XM_017024025.1:c.714T>C	XP_016879514.1:p.Ser238=
XM_017024026.1:c.714T>C	XP_016879515.1:p.Ser238=
XM_017024027.1:c.714T>C	XP_016879516.1:p.Ser238=
XM_017024028.2:c.714T>C	XP_016879517.1:p.Ser238=
NM_030665.4:c.714T>C MANE Select	NP_109590.3:p.Ser238=