Canonical Allele Identifier: CA500989433
Gene: DLX3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.48069193G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49991829G>A , CM000679.2:g.49991829G>A GRCh38
NC_000017.10:g.48069193G>A , CM000679.1:g.48069193G>A GRCh37
NC_000017.9:g.45424192G>A NCBI36
NG_023063.1:g.8396C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000434704.2:c.552C>T MANE Select ENSP00000389870.2:p.Phe184=
ENST00000512495.2:c.192C>T ENSP00000449976.1:p.Phe64=
NM_005220.2:c.552C>T NP_005211.1:p.Phe184=
XM_011524458.1:c.516+1571C>T XP_011522760.1:n.516+1571C>T
NM_005220.3:c.552C>T MANE Select NP_005211.1:p.Phe184=