Canonical Allele Identifier: CA2638666533

Gene: DLX4

Linked Data

• gnomAD v4: 17-49974236-CTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49974238_49974239del , CM000679.2:g.49974238_49974239del	GRCh38
NC_000017.10:g.48051602_48051603del , CM000679.1:g.48051602_48051603del	GRCh37
NC_000017.9:g.45406601_45406602del	NCBI36
NG_030592.1:g.10041_10042del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706528.1:n.1899_1900del
ENST00000240306.5:c.*295_*296del MANE Select	ENSP00000240306.3:n.*295_*296del
ENST00000240306.4:c.*295_*296del	ENSP00000240306.3:n.*295_*296del
ENST00000411890.3:c.*295_*296del	ENSP00000410622.2:n.*295_*296del
ENST00000611342.1:c.*888_*889del	ENSP00000480366.1:n.*888_*889del
NM_001934.3:c.*295_*296del	NP_001925.2:n.*295_*296del
NM_138281.2:c.*295_*296del	NP_612138.1:n.*295_*296del
XM_011524459.1:c.*295_*296del	XP_011522761.1:n.*295_*296del
XM_017024291.1:c.*295_*296del	XP_016879780.1:n.*295_*296del
NM_138281.3:c.*295_*296del MANE Select	NP_612138.1:n.*295_*296del
NM_001934.4:c.*295_*296del	NP_001925.2:n.*295_*296del