Canonical Allele Identifier: CA291506303
Gene: DLX3 HGNC NCBI

Linked Data

dbSNP Id: rs544889964

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49991723A>G , CM000679.2:g.49991723A>G GRCh38
NC_000017.10:g.48069087A>G , CM000679.1:g.48069087A>G GRCh37
NC_000017.9:g.45424086A>G NCBI36
NG_023063.1:g.8502T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000434704.2:c.658T>C MANE Select ENSP00000389870.2:p.Ser220Pro
ENST00000512495.2:c.298T>C ENSP00000449976.1:p.Ser100Pro
NM_005220.2:c.658T>C NP_005211.1:p.Ser220Pro
XM_011524458.1:c.516+1677T>C XP_011522760.1:n.516+1677T>C
NM_005220.3:c.658T>C MANE Select NP_005211.1:p.Ser220Pro