Canonical Allele Identifier: CA2263813886

Gene: DLX4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49973885T= , CM000679.2:g.49973885T=	GRCh38
NC_000017.10:g.48051249T= , CM000679.1:g.48051249T=	GRCh37
NC_000017.9:g.45406248T=	NCBI36
NG_030592.1:g.9688T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706528.1:n.1546T=
ENST00000240306.5:c.665T= MANE Select	ENSP00000240306.3:p.Phe222=
ENST00000240306.4:c.665T=	ENSP00000240306.3:p.Phe222=
ENST00000411890.3:c.449T=	ENSP00000410622.2:p.Phe150=
ENST00000611342.1:c.*535T=	ENSP00000480366.1:n.*535T=
NM_001934.3:c.449T=	NP_001925.2:p.Phe150=
NM_138281.2:c.665T=	NP_612138.1:p.Phe222=
XM_011524459.1:c.449T=	XP_011522761.1:p.Phe150=
XM_017024291.1:c.449T=	XP_016879780.1:p.Phe150=
NM_138281.3:c.665T= MANE Select	NP_612138.1:p.Phe222=
NM_001934.4:c.449T=	NP_001925.2:p.Phe150=