Canonical Allele Identifier: CA2638666134

Gene: DLX4

Linked Data

• gnomAD v4: 17-49973798-CTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49973802_49973803del , CM000679.2:g.49973802_49973803del	GRCh38
NC_000017.10:g.48051166_48051167del , CM000679.1:g.48051166_48051167del	GRCh37
NC_000017.9:g.45406165_45406166del	NCBI36
NG_030592.1:g.9605_9606del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706528.1:n.1463_1464del
ENST00000240306.5:c.582_583del MANE Select	ENSP00000240306.3:p.Pro196LeufsTer?
ENST00000240306.4:c.582_583del	ENSP00000240306.3:p.Pro196LeufsTer?
ENST00000411890.3:c.366_367del	ENSP00000410622.2:p.Pro124LeufsTer?
ENST00000611342.1:c.*452_*453del	ENSP00000480366.1:n.*452_*453del
NM_001934.3:c.366_367del	NP_001925.2:p.Pro124LeufsTer?
NM_138281.2:c.582_583del	NP_612138.1:p.Pro196LeufsTer?
XM_011524459.1:c.366_367del	XP_011522761.1:p.Pro124LeufsTer?
XM_017024291.1:c.366_367del	XP_016879780.1:p.Pro124LeufsTer?
NM_138281.3:c.582_583del MANE Select	NP_612138.1:p.Pro196LeufsTer?
NM_001934.4:c.366_367del	NP_001925.2:p.Pro124LeufsTer?