Canonical Allele Identifier: CA400173930
Gene: DLX3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.48069086G>T (hg19) chr17:g.49991722G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49991722G>T , CM000679.2:g.49991722G>T GRCh38
NC_000017.10:g.48069086G>T , CM000679.1:g.48069086G>T GRCh37
NC_000017.9:g.45424085G>T NCBI36
NG_023063.1:g.8503C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000434704.2:c.659C>A MANE Select ENSP00000389870.2:p.Ser220Tyr
ENST00000512495.2:c.299C>A ENSP00000449976.1:p.Ser100Tyr
NM_005220.2:c.659C>A NP_005211.1:p.Ser220Tyr
XM_011524458.1:c.516+1678C>A XP_011522760.1:n.516+1678C>A
NM_005220.3:c.659C>A MANE Select NP_005211.1:p.Ser220Tyr
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