Canonical Allele Identifier: CA2263823568
Gene: DLX3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49995032T= , CM000679.2:g.49995032T= GRCh38
NC_000017.10:g.48072396T= , CM000679.1:g.48072396T= GRCh37
NC_000017.9:g.45427395T= NCBI36
NG_023063.1:g.5193A=

Transcript Alleles

HGVS Amino-acid change
ENST00000434704.2:c.-34A= MANE Select ENSP00000389870.2:n.-34A=
NM_005220.2:c.-34A= NP_005211.1:n.-34A=
XM_011524458.1:c.-34A= XP_011522760.1:n.-34A=
NM_005220.3:c.-34A= MANE Select NP_005211.1:n.-34A=