Canonical Allele Identifier: CA2638666313

Gene: DLX4

Linked Data

• gnomAD v4: 17-49974109-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49974109A>C , CM000679.2:g.49974109A>C	GRCh38
NC_000017.10:g.48051473A>C , CM000679.1:g.48051473A>C	GRCh37
NC_000017.9:g.45406472A>C	NCBI36
NG_030592.1:g.9912A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706528.1:n.1770A>C
ENST00000240306.5:c.*166A>C MANE Select	ENSP00000240306.3:n.*166A>C
ENST00000240306.4:c.*166A>C	ENSP00000240306.3:n.*166A>C
ENST00000411890.3:c.*166A>C	ENSP00000410622.2:n.*166A>C
ENST00000611342.1:c.*759A>C	ENSP00000480366.1:n.*759A>C
NM_001934.3:c.*166A>C	NP_001925.2:n.*166A>C
NM_138281.2:c.*166A>C	NP_612138.1:n.*166A>C
XM_011524459.1:c.*166A>C	XP_011522761.1:n.*166A>C
XM_017024291.1:c.*166A>C	XP_016879780.1:n.*166A>C
NM_138281.3:c.*166A>C MANE Select	NP_612138.1:n.*166A>C
NM_001934.4:c.*166A>C	NP_001925.2:n.*166A>C