Canonical Allele Identifier: CA500989074

Gene: DLX4

Linked Data

• MyVariant Identifiers: chr17:g.48051289T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49973925T>A , CM000679.2:g.49973925T>A	GRCh38
NC_000017.10:g.48051289T>A , CM000679.1:g.48051289T>A	GRCh37
NC_000017.9:g.45406288T>A	NCBI36
NG_030592.1:g.9728T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706528.1:n.1586T>A
ENST00000240306.5:c.705T>A MANE Select	ENSP00000240306.3:p.Ala235=
ENST00000240306.4:c.705T>A	ENSP00000240306.3:p.Ala235=
ENST00000411890.3:c.489T>A	ENSP00000410622.2:p.Ala163=
ENST00000611342.1:c.*575T>A	ENSP00000480366.1:n.*575T>A
NM_001934.3:c.489T>A	NP_001925.2:p.Ala163=
NM_138281.2:c.705T>A	NP_612138.1:p.Ala235=
XM_011524459.1:c.489T>A	XP_011522761.1:p.Ala163=
XM_017024291.1:c.489T>A	XP_016879780.1:p.Ala163=
NM_138281.3:c.705T>A MANE Select	NP_612138.1:p.Ala235=
NM_001934.4:c.489T>A	NP_001925.2:p.Ala163=