Canonical Allele Identifier: CA498422823

Gene: RAI1

Linked Data

• ClinVar Variation Id: 1588323
• ClinVar RCV Id: RCV002096017
• dbSNP Id: rs2143001636
• gnomAD v4: 17-17793542-C-T
• COSMIC: COSM4501631 ; COSM4501632
• MyVariant Identifiers: chr17:g.17696856C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17793542C>T , CM000679.2:g.17793542C>T	GRCh38
NC_000017.10:g.17696856C>T , CM000679.1:g.17696856C>T	GRCh37
NC_000017.9:g.17637581C>T	NCBI36
NG_007101.2:g.117070C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000353383.6:c.594C>T MANE Select	ENSP00000323074.4:p.Ala198=
ENST00000640861.1:c.594C>T	ENSP00000491773.1:p.Ala198=
ENST00000353383.5:c.594C>T	ENSP00000323074.4:p.Ala198=
ENST00000395774.1:c.594C>T	ENSP00000379120.1:p.Ala198=
NM_030665.3:c.594C>T	NP_109590.3:p.Ala198=
XM_017024025.1:c.594C>T	XP_016879514.1:p.Ala198=
XM_017024026.1:c.594C>T	XP_016879515.1:p.Ala198=
XM_017024027.1:c.594C>T	XP_016879516.1:p.Ala198=
XM_017024028.2:c.594C>T	XP_016879517.1:p.Ala198=
NM_030665.4:c.594C>T MANE Select	NP_109590.3:p.Ala198=