Canonical Allele Identifier: CA2263813881
Gene: DLX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49973865C= , CM000679.2:g.49973865C= GRCh38
NC_000017.10:g.48051229C= , CM000679.1:g.48051229C= GRCh37
NC_000017.9:g.45406228C= NCBI36
NG_030592.1:g.9668C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706528.1:n.1526C=
ENST00000240306.5:c.645C= MANE Select ENSP00000240306.3:p.Thr215=
ENST00000240306.4:c.645C= ENSP00000240306.3:p.Thr215=
ENST00000411890.3:c.429C= ENSP00000410622.2:p.Thr143=
ENST00000611342.1:c.*515C= ENSP00000480366.1:n.*515C=
NM_001934.3:c.429C= NP_001925.2:p.Thr143=
NM_138281.2:c.645C= NP_612138.1:p.Thr215=
XM_011524459.1:c.429C= XP_011522761.1:p.Thr143=
XM_017024291.1:c.429C= XP_016879780.1:p.Thr143=
NM_138281.3:c.645C= MANE Select NP_612138.1:p.Thr215=
NM_001934.4:c.429C= NP_001925.2:p.Thr143=