Canonical Allele Identifier: CA2638666541

Gene: DLX4

Linked Data

• gnomAD v4: 17-49974239-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49974239T>G , CM000679.2:g.49974239T>G	GRCh38
NC_000017.10:g.48051603T>G , CM000679.1:g.48051603T>G	GRCh37
NC_000017.9:g.45406602T>G	NCBI36
NG_030592.1:g.10042T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706528.1:n.1900T>G
ENST00000240306.5:c.*296T>G MANE Select	ENSP00000240306.3:n.*296T>G
ENST00000240306.4:c.*296T>G	ENSP00000240306.3:n.*296T>G
ENST00000411890.3:c.*296T>G	ENSP00000410622.2:n.*296T>G
ENST00000611342.1:c.*889T>G	ENSP00000480366.1:n.*889T>G
NM_001934.3:c.*296T>G	NP_001925.2:n.*296T>G
NM_138281.2:c.*296T>G	NP_612138.1:n.*296T>G
XM_011524459.1:c.*296T>G	XP_011522761.1:n.*296T>G
XM_017024291.1:c.*296T>G	XP_016879780.1:n.*296T>G
NM_138281.3:c.*296T>G MANE Select	NP_612138.1:n.*296T>G
NM_001934.4:c.*296T>G	NP_001925.2:n.*296T>G