Canonical Allele Identifier: CA2263814057

Gene: DLX4

Linked Data

• dbSNP Id: rs1905638506
• gnomAD v4: 17-49974273-CCTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49974278_49974280del , CM000679.2:g.49974278_49974280del	GRCh38
NC_000017.10:g.48051642_48051644del , CM000679.1:g.48051642_48051644del	GRCh37
NC_000017.9:g.45406641_45406643del	NCBI36
NG_030592.1:g.10081_10083del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706528.1:n.1939_1941del
ENST00000240306.5:c.*335_*337del MANE Select	ENSP00000240306.3:n.*335_*337del
ENST00000240306.4:c.*335_*337del	ENSP00000240306.3:n.*335_*337del
ENST00000411890.3:c.*335_*337del	ENSP00000410622.2:n.*335_*337del
ENST00000611342.1:c.*928_*930del	ENSP00000480366.1:n.*928_*930del
NM_001934.3:c.*335_*337del	NP_001925.2:n.*335_*337del
NM_138281.2:c.*335_*337del	NP_612138.1:n.*335_*337del
XM_011524459.1:c.*335_*337del	XP_011522761.1:n.*335_*337del
XM_017024291.1:c.*335_*337del	XP_016879780.1:n.*335_*337del
NM_138281.3:c.*335_*337del MANE Select	NP_612138.1:n.*335_*337del
NM_001934.4:c.*335_*337del	NP_001925.2:n.*335_*337del