Canonical Allele Identifier: CA2638666188

Gene: DLX4

Linked Data

• gnomAD v4: 17-49974012-C-CAG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49974012_49974013insAG , CM000679.2:g.49974012_49974013insAG	GRCh38
NC_000017.10:g.48051376_48051377insAG , CM000679.1:g.48051376_48051377insAG	GRCh37
NC_000017.9:g.45406375_45406376insAG	NCBI36
NG_030592.1:g.9815_9816insAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706528.1:n.1673_1674insAG
ENST00000240306.5:c.*69_*70insAG MANE Select	ENSP00000240306.3:n.*69_*70insAG
ENST00000240306.4:c.*69_*70insAG	ENSP00000240306.3:n.*69_*70insAG
ENST00000411890.3:c.*69_*70insAG	ENSP00000410622.2:n.*69_*70insAG
ENST00000611342.1:c.*662_*663insAG	ENSP00000480366.1:n.*662_*663insAG
NM_001934.3:c.*69_*70insAG	NP_001925.2:n.*69_*70insAG
NM_138281.2:c.*69_*70insAG	NP_612138.1:n.*69_*70insAG
XM_011524459.1:c.*69_*70insAG	XP_011522761.1:n.*69_*70insAG
XM_017024291.1:c.*69_*70insAG	XP_016879780.1:n.*69_*70insAG
NM_138281.3:c.*69_*70insAG MANE Select	NP_612138.1:n.*69_*70insAG
NM_001934.4:c.*69_*70insAG	NP_001925.2:n.*69_*70insAG