Canonical Allele Identifier: CA2263813864
Gene: DLX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49973832_49973833delinsCT , CM000679.2:g.49973832_49973833delinsCT GRCh38
NC_000017.10:g.48051196_48051197delinsCT , CM000679.1:g.48051196_48051197delinsCT GRCh37
NC_000017.9:g.45406195_45406196delinsCT NCBI36
NG_030592.1:g.9635_9636delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000706528.1:n.1493_1494delinsCT
ENST00000240306.5:c.612_613delinsCT MANE Select ENSP00000240306.3:p.Leu204=
ENST00000240306.4:c.612_613delinsCT ENSP00000240306.3:p.Leu204=
ENST00000411890.3:c.396_397delinsCT ENSP00000410622.2:p.Leu132=
ENST00000611342.1:c.*482_*483delinsCT ENSP00000480366.1:n.*482_*483delinsCT
NM_001934.3:c.396_397delinsCT NP_001925.2:p.Leu132=
NM_138281.2:c.612_613delinsCT NP_612138.1:p.Leu204=
XM_011524459.1:c.396_397delinsCT XP_011522761.1:p.Leu132=
XM_017024291.1:c.396_397delinsCT XP_016879780.1:p.Leu132=
NM_138281.3:c.612_613delinsCT MANE Select NP_612138.1:p.Leu204=
NM_001934.4:c.396_397delinsCT NP_001925.2:p.Leu132=