Canonical Allele Identifier: CA2263813999

Gene: DLX4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49974144A= , CM000679.2:g.49974144A=	GRCh38
NC_000017.10:g.48051508A= , CM000679.1:g.48051508A=	GRCh37
NC_000017.9:g.45406507A=	NCBI36
NG_030592.1:g.9947A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706528.1:n.1805A=
ENST00000240306.5:c.*201A= MANE Select	ENSP00000240306.3:n.*201A=
ENST00000240306.4:c.*201A=	ENSP00000240306.3:n.*201A=
ENST00000411890.3:c.*201A=	ENSP00000410622.2:n.*201A=
ENST00000611342.1:c.*794A=	ENSP00000480366.1:n.*794A=
NM_001934.3:c.*201A=	NP_001925.2:n.*201A=
NM_138281.2:c.*201A=	NP_612138.1:n.*201A=
XM_011524459.1:c.*201A=	XP_011522761.1:n.*201A=
XM_017024291.1:c.*201A=	XP_016879780.1:n.*201A=
NM_138281.3:c.*201A= MANE Select	NP_612138.1:n.*201A=
NM_001934.4:c.*201A=	NP_001925.2:n.*201A=