Canonical Allele Identifier: CA400173985
Gene: DLX3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.48069094G>C (hg19) chr17:g.49991730G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49991730G>C , CM000679.2:g.49991730G>C GRCh38
NC_000017.10:g.48069094G>C , CM000679.1:g.48069094G>C GRCh37
NC_000017.9:g.45424093G>C NCBI36
NG_023063.1:g.8495C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000434704.2:c.651C>G MANE Select ENSP00000389870.2:p.Asp217Glu
ENST00000512495.2:c.291C>G ENSP00000449976.1:p.Asp97Glu
NM_005220.2:c.651C>G NP_005211.1:p.Asp217Glu
XM_011524458.1:c.516+1670C>G XP_011522760.1:n.516+1670C>G
NM_005220.3:c.651C>G MANE Select NP_005211.1:p.Asp217Glu
Search 100 bp 5'
Search 100 bp 3'