Canonical Allele Identifier: CA398546134
Gene: RAI1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.17697014T>A (hg19) chr17:g.17793700T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.17793700T>A , CM000679.2:g.17793700T>A GRCh38
NC_000017.10:g.17697014T>A , CM000679.1:g.17697014T>A GRCh37
NC_000017.9:g.17637739T>A NCBI36
NG_007101.2:g.117228T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000353383.6:c.752T>A MANE Select ENSP00000323074.4:p.Leu251Gln
ENST00000640861.1:c.686T>A ENSP00000491773.1:p.Leu229Gln
ENST00000353383.5:c.752T>A ENSP00000323074.4:p.Leu251Gln
ENST00000395774.1:c.752T>A ENSP00000379120.1:p.Leu251Gln
NM_030665.3:c.752T>A NP_109590.3:p.Leu251Gln
XM_017024025.1:c.752T>A XP_016879514.1:p.Leu251Gln
XM_017024026.1:c.752T>A XP_016879515.1:p.Leu251Gln
XM_017024027.1:c.752T>A XP_016879516.1:p.Leu251Gln
XM_017024028.2:c.752T>A XP_016879517.1:p.Leu251Gln
NM_030665.4:c.752T>A MANE Select NP_109590.3:p.Leu251Gln
Search 100 bp 5'
Search 100 bp 3'