Canonical Allele Identifier: CA500989439
Gene: DLX3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.48069199G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49991835G>T , CM000679.2:g.49991835G>T GRCh38
NC_000017.10:g.48069199G>T , CM000679.1:g.48069199G>T GRCh37
NC_000017.9:g.45424198G>T NCBI36
NG_023063.1:g.8390C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000434704.2:c.546C>A MANE Select ENSP00000389870.2:p.Ser182=
ENST00000512495.2:c.186C>A ENSP00000449976.1:p.Ser62=
NM_005220.2:c.546C>A NP_005211.1:p.Ser182=
XM_011524458.1:c.516+1565C>A XP_011522760.1:n.516+1565C>A
NM_005220.3:c.546C>A MANE Select NP_005211.1:p.Ser182=