Canonical Allele Identifier: CA2263813898

Gene: DLX4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49973907C= , CM000679.2:g.49973907C=	GRCh38
NC_000017.10:g.48051271C= , CM000679.1:g.48051271C=	GRCh37
NC_000017.9:g.45406270C=	NCBI36
NG_030592.1:g.9710C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706528.1:n.1568C=
ENST00000240306.5:c.687C= MANE Select	ENSP00000240306.3:p.His229=
ENST00000240306.4:c.687C=	ENSP00000240306.3:p.His229=
ENST00000411890.3:c.471C=	ENSP00000410622.2:p.His157=
ENST00000611342.1:c.*557C=	ENSP00000480366.1:n.*557C=
NM_001934.3:c.471C=	NP_001925.2:p.His157=
NM_138281.2:c.687C=	NP_612138.1:p.His229=
XM_011524459.1:c.471C=	XP_011522761.1:p.His157=
XM_017024291.1:c.471C=	XP_016879780.1:p.His157=
NM_138281.3:c.687C= MANE Select	NP_612138.1:p.His229=
NM_001934.4:c.471C=	NP_001925.2:p.His157=