Canonical Allele Identifier: CA400168655

Gene: DLX4

Linked Data

• MyVariant Identifiers: chr17:g.48051236T>G (hg19) ; chr17:g.49973872T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49973872T>G , CM000679.2:g.49973872T>G	GRCh38
NC_000017.10:g.48051236T>G , CM000679.1:g.48051236T>G	GRCh37
NC_000017.9:g.45406235T>G	NCBI36
NG_030592.1:g.9675T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706528.1:n.1533T>G
ENST00000240306.5:c.652T>G MANE Select	ENSP00000240306.3:p.Tyr218Asp
ENST00000240306.4:c.652T>G	ENSP00000240306.3:p.Tyr218Asp
ENST00000411890.3:c.436T>G	ENSP00000410622.2:p.Tyr146Asp
ENST00000611342.1:c.*522T>G	ENSP00000480366.1:n.*522T>G
NM_001934.3:c.436T>G	NP_001925.2:p.Tyr146Asp
NM_138281.2:c.652T>G	NP_612138.1:p.Tyr218Asp
XM_011524459.1:c.436T>G	XP_011522761.1:p.Tyr146Asp
XM_017024291.1:c.436T>G	XP_016879780.1:p.Tyr146Asp
NM_138281.3:c.652T>G MANE Select	NP_612138.1:p.Tyr218Asp
NM_001934.4:c.436T>G	NP_001925.2:p.Tyr146Asp