Canonical Allele Identifier: CA8418143
Gene: RAI1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1200133
ClinVar RCV Id: RCV001565052 RCV003910885
dbSNP Id: rs753632651
ExAC: 17:17696792 C / T
gnomAD v2: 17-17696792-C-T
gnomAD v3: 17-17793478-C-T
gnomAD v4: 17-17793478-C-T
MyVariant Identifiers: chr17:g.17696792C>T (hg19) chr17:g.17793478C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.17793478C>T , CM000679.2:g.17793478C>T GRCh38
NC_000017.10:g.17696792C>T , CM000679.1:g.17696792C>T GRCh37
NC_000017.9:g.17637517C>T NCBI36
NG_007101.2:g.117006C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000353383.6:c.530C>T MANE Select ENSP00000323074.4:p.Pro177Leu
ENST00000640861.1:c.530C>T ENSP00000491773.1:p.Pro177Leu
ENST00000353383.5:c.530C>T ENSP00000323074.4:p.Pro177Leu
ENST00000395774.1:c.530C>T ENSP00000379120.1:p.Pro177Leu
NM_030665.3:c.530C>T NP_109590.3:p.Pro177Leu
XM_017024025.1:c.530C>T XP_016879514.1:p.Pro177Leu
XM_017024026.1:c.530C>T XP_016879515.1:p.Pro177Leu
XM_017024027.1:c.530C>T XP_016879516.1:p.Pro177Leu
XM_017024028.2:c.530C>T XP_016879517.1:p.Pro177Leu
NM_030665.4:c.530C>T MANE Select NP_109590.3:p.Pro177Leu
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