Canonical Allele Identifier: CA2263813878
Gene: DLX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49973854A= , CM000679.2:g.49973854A= GRCh38
NC_000017.10:g.48051218A= , CM000679.1:g.48051218A= GRCh37
NC_000017.9:g.45406217A= NCBI36
NG_030592.1:g.9657A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706528.1:n.1515A=
ENST00000240306.5:c.634A= MANE Select ENSP00000240306.3:p.Thr212=
ENST00000240306.4:c.634A= ENSP00000240306.3:p.Thr212=
ENST00000411890.3:c.418A= ENSP00000410622.2:p.Thr140=
ENST00000611342.1:c.*504A= ENSP00000480366.1:n.*504A=
NM_001934.3:c.418A= NP_001925.2:p.Thr140=
NM_138281.2:c.634A= NP_612138.1:p.Thr212=
XM_011524459.1:c.418A= XP_011522761.1:p.Thr140=
XM_017024291.1:c.418A= XP_016879780.1:p.Thr140=
NM_138281.3:c.634A= MANE Select NP_612138.1:p.Thr212=
NM_001934.4:c.418A= NP_001925.2:p.Thr140=