Canonical Allele Identifier: CA500989045

Gene: DLX4

Linked Data

• MyVariant Identifiers: chr17:g.48051157C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49973793C>G , CM000679.2:g.49973793C>G	GRCh38
NC_000017.10:g.48051157C>G , CM000679.1:g.48051157C>G	GRCh37
NC_000017.9:g.45406156C>G	NCBI36
NG_030592.1:g.9596C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706528.1:n.1454C>G
ENST00000240306.5:c.573C>G MANE Select	ENSP00000240306.3:p.Thr191=
ENST00000240306.4:c.573C>G	ENSP00000240306.3:p.Thr191=
ENST00000411890.3:c.357C>G	ENSP00000410622.2:p.Thr119=
ENST00000611342.1:c.*443C>G	ENSP00000480366.1:n.*443C>G
NM_001934.3:c.357C>G	NP_001925.2:p.Thr119=
NM_138281.2:c.573C>G	NP_612138.1:p.Thr191=
XM_011524459.1:c.357C>G	XP_011522761.1:p.Thr119=
XM_017024291.1:c.357C>G	XP_016879780.1:p.Thr119=
NM_138281.3:c.573C>G MANE Select	NP_612138.1:p.Thr191=
NM_001934.4:c.357C>G	NP_001925.2:p.Thr119=