Canonical Allele Identifier: CA398545815

Gene: RAI1

Linked Data

• ClinVar Variation Id: 2698776
• ClinVar RCV Id: RCV003544309
• dbSNP Id: rs560444397
• gnomAD v3: 17-17793546-C-G
• gnomAD v4: 17-17793546-C-G
• MyVariant Identifiers: chr17:g.17696860C>G (hg19) ; chr17:g.17793546C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17793546C>G , CM000679.2:g.17793546C>G	GRCh38
NC_000017.10:g.17696860C>G , CM000679.1:g.17696860C>G	GRCh37
NC_000017.9:g.17637585C>G	NCBI36
NG_007101.2:g.117074C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000353383.6:c.598C>G MANE Select	ENSP00000323074.4:p.Pro200Ala
ENST00000640861.1:c.598C>G	ENSP00000491773.1:p.Pro200Ala
ENST00000353383.5:c.598C>G	ENSP00000323074.4:p.Pro200Ala
ENST00000395774.1:c.598C>G	ENSP00000379120.1:p.Pro200Ala
NM_030665.3:c.598C>G	NP_109590.3:p.Pro200Ala
XM_017024025.1:c.598C>G	XP_016879514.1:p.Pro200Ala
XM_017024026.1:c.598C>G	XP_016879515.1:p.Pro200Ala
XM_017024027.1:c.598C>G	XP_016879516.1:p.Pro200Ala
XM_017024028.2:c.598C>G	XP_016879517.1:p.Pro200Ala
NM_030665.4:c.598C>G MANE Select	NP_109590.3:p.Pro200Ala