Canonical Allele Identifier: CA2638666455

Gene: DLX4

Linked Data

• gnomAD v4: 17-49974189-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49974189C>A , CM000679.2:g.49974189C>A	GRCh38
NC_000017.10:g.48051553C>A , CM000679.1:g.48051553C>A	GRCh37
NC_000017.9:g.45406552C>A	NCBI36
NG_030592.1:g.9992C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706528.1:n.1850C>A
ENST00000240306.5:c.*246C>A MANE Select	ENSP00000240306.3:n.*246C>A
ENST00000240306.4:c.*246C>A	ENSP00000240306.3:n.*246C>A
ENST00000411890.3:c.*246C>A	ENSP00000410622.2:n.*246C>A
ENST00000611342.1:c.*839C>A	ENSP00000480366.1:n.*839C>A
NM_001934.3:c.*246C>A	NP_001925.2:n.*246C>A
NM_138281.2:c.*246C>A	NP_612138.1:n.*246C>A
XM_011524459.1:c.*246C>A	XP_011522761.1:n.*246C>A
XM_017024291.1:c.*246C>A	XP_016879780.1:n.*246C>A
NM_138281.3:c.*246C>A MANE Select	NP_612138.1:n.*246C>A
NM_001934.4:c.*246C>A	NP_001925.2:n.*246C>A