Canonical Allele Identifier: CA398545905

Gene: RAI1

Linked Data

• ClinVar Variation Id: 2635556
• ClinVar RCV Id: RCV003410591
• dbSNP Id: rs2032105178
• gnomAD v3: 17-17793588-C-T
• gnomAD v4: 17-17793588-C-T
• MyVariant Identifiers: chr17:g.17696902C>T (hg19) ; chr17:g.17793588C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.17793588C>T , CM000679.2:g.17793588C>T	GRCh38
NC_000017.10:g.17696902C>T , CM000679.1:g.17696902C>T	GRCh37
NC_000017.9:g.17637627C>T	NCBI36
NG_007101.2:g.117116C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000353383.6:c.640C>T MANE Select	ENSP00000323074.4:p.Gln214Ter
ENST00000640861.1:c.616+24C>T	ENSP00000491773.1:n.616+24C>T
ENST00000353383.5:c.640C>T	ENSP00000323074.4:p.Gln214Ter
ENST00000395774.1:c.640C>T	ENSP00000379120.1:p.Gln214Ter
NM_030665.3:c.640C>T	NP_109590.3:p.Gln214Ter
XM_017024025.1:c.640C>T	XP_016879514.1:p.Gln214Ter
XM_017024026.1:c.640C>T	XP_016879515.1:p.Gln214Ter
XM_017024027.1:c.640C>T	XP_016879516.1:p.Gln214Ter
XM_017024028.2:c.640C>T	XP_016879517.1:p.Gln214Ter
NM_030665.4:c.640C>T MANE Select	NP_109590.3:p.Gln214Ter