Canonical Allele Identifier: CA2638666356

Gene: DLX4

Linked Data

• gnomAD v4: 17-49974138-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49974138C>A , CM000679.2:g.49974138C>A	GRCh38
NC_000017.10:g.48051502C>A , CM000679.1:g.48051502C>A	GRCh37
NC_000017.9:g.45406501C>A	NCBI36
NG_030592.1:g.9941C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706528.1:n.1799C>A
ENST00000240306.5:c.*195C>A MANE Select	ENSP00000240306.3:n.*195C>A
ENST00000240306.4:c.*195C>A	ENSP00000240306.3:n.*195C>A
ENST00000411890.3:c.*195C>A	ENSP00000410622.2:n.*195C>A
ENST00000611342.1:c.*788C>A	ENSP00000480366.1:n.*788C>A
NM_001934.3:c.*195C>A	NP_001925.2:n.*195C>A
NM_138281.2:c.*195C>A	NP_612138.1:n.*195C>A
XM_011524459.1:c.*195C>A	XP_011522761.1:n.*195C>A
XM_017024291.1:c.*195C>A	XP_016879780.1:n.*195C>A
NM_138281.3:c.*195C>A MANE Select	NP_612138.1:n.*195C>A
NM_001934.4:c.*195C>A	NP_001925.2:n.*195C>A