Canonical Allele Identifier: CA398546343

Gene: RAI1

Linked Data

• ClinVar Variation Id: 1368467
• ClinVar RCV Id: RCV001874418
• dbSNP Id: rs1044807296
• MyVariant Identifiers: chr17:g.17697114G>C (hg19) ; chr17:g.17793800G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17793800G>C , CM000679.2:g.17793800G>C	GRCh38
NC_000017.10:g.17697114G>C , CM000679.1:g.17697114G>C	GRCh37
NC_000017.9:g.17637839G>C	NCBI36
NG_007101.2:g.117328G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000353383.6:c.852G>C MANE Select	ENSP00000323074.4:p.Gln284His
ENST00000640861.1:c.786G>C	ENSP00000491773.1:p.Gln262His
ENST00000353383.5:c.852G>C	ENSP00000323074.4:p.Gln284His
ENST00000395774.1:c.852G>C	ENSP00000379120.1:p.Gln284His
NM_030665.3:c.852G>C	NP_109590.3:p.Gln284His
XM_017024025.1:c.852G>C	XP_016879514.1:p.Gln284His
XM_017024026.1:c.852G>C	XP_016879515.1:p.Gln284His
XM_017024027.1:c.852G>C	XP_016879516.1:p.Gln284His
XM_017024028.2:c.852G>C	XP_016879517.1:p.Gln284His
NM_030665.4:c.852G>C MANE Select	NP_109590.3:p.Gln284His