Canonical Allele Identifier: CA398546277
Gene: RAI1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.17697086G>A (hg19) chr17:g.17793772G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.17793772G>A , CM000679.2:g.17793772G>A GRCh38
NC_000017.10:g.17697086G>A , CM000679.1:g.17697086G>A GRCh37
NC_000017.9:g.17637811G>A NCBI36
NG_007101.2:g.117300G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000353383.6:c.824G>A MANE Select ENSP00000323074.4:p.Ser275Asn
ENST00000640861.1:c.758G>A ENSP00000491773.1:p.Ser253Asn
ENST00000353383.5:c.824G>A ENSP00000323074.4:p.Ser275Asn
ENST00000395774.1:c.824G>A ENSP00000379120.1:p.Ser275Asn
NM_030665.3:c.824G>A NP_109590.3:p.Ser275Asn
XM_017024025.1:c.824G>A XP_016879514.1:p.Ser275Asn
XM_017024026.1:c.824G>A XP_016879515.1:p.Ser275Asn
XM_017024027.1:c.824G>A XP_016879516.1:p.Ser275Asn
XM_017024028.2:c.824G>A XP_016879517.1:p.Ser275Asn
NM_030665.4:c.824G>A MANE Select NP_109590.3:p.Ser275Asn
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