Canonical Allele Identifier: CA500989000

Gene: DLX4

Linked Data

• MyVariant Identifiers: chr17:g.48051229C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49973865C>A , CM000679.2:g.49973865C>A	GRCh38
NC_000017.10:g.48051229C>A , CM000679.1:g.48051229C>A	GRCh37
NC_000017.9:g.45406228C>A	NCBI36
NG_030592.1:g.9668C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706528.1:n.1526C>A
ENST00000240306.5:c.645C>A MANE Select	ENSP00000240306.3:p.Thr215=
ENST00000240306.4:c.645C>A	ENSP00000240306.3:p.Thr215=
ENST00000411890.3:c.429C>A	ENSP00000410622.2:p.Thr143=
ENST00000611342.1:c.*515C>A	ENSP00000480366.1:n.*515C>A
NM_001934.3:c.429C>A	NP_001925.2:p.Thr143=
NM_138281.2:c.645C>A	NP_612138.1:p.Thr215=
XM_011524459.1:c.429C>A	XP_011522761.1:p.Thr143=
XM_017024291.1:c.429C>A	XP_016879780.1:p.Thr143=
NM_138281.3:c.645C>A MANE Select	NP_612138.1:p.Thr215=
NM_001934.4:c.429C>A	NP_001925.2:p.Thr143=