Canonical Allele Identifier: CA2638666593

Gene: DLX4

Linked Data

• gnomAD v4: 17-49974264-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49974269del , CM000679.2:g.49974269del	GRCh38
NC_000017.10:g.48051633del , CM000679.1:g.48051633del	GRCh37
NC_000017.9:g.45406632del	NCBI36
NG_030592.1:g.10072del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706528.1:n.1930del
ENST00000240306.5:c.*326del MANE Select	ENSP00000240306.3:n.*326del
ENST00000240306.4:c.*326del	ENSP00000240306.3:n.*326del
ENST00000411890.3:c.*326del	ENSP00000410622.2:n.*326del
ENST00000611342.1:c.*919del	ENSP00000480366.1:n.*919del
NM_001934.3:c.*326del	NP_001925.2:n.*326del
NM_138281.2:c.*326del	NP_612138.1:n.*326del
XM_011524459.1:c.*326del	XP_011522761.1:n.*326del
XM_017024291.1:c.*326del	XP_016879780.1:n.*326del
NM_138281.3:c.*326del MANE Select	NP_612138.1:n.*326del
NM_001934.4:c.*326del	NP_001925.2:n.*326del