Canonical Allele Identifier: CA2638666373

Gene: DLX4

Linked Data

• gnomAD v4: 17-49974153-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49974153G>C , CM000679.2:g.49974153G>C	GRCh38
NC_000017.10:g.48051517G>C , CM000679.1:g.48051517G>C	GRCh37
NC_000017.9:g.45406516G>C	NCBI36
NG_030592.1:g.9956G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706528.1:n.1814G>C
ENST00000240306.5:c.*210G>C MANE Select	ENSP00000240306.3:n.*210G>C
ENST00000240306.4:c.*210G>C	ENSP00000240306.3:n.*210G>C
ENST00000411890.3:c.*210G>C	ENSP00000410622.2:n.*210G>C
ENST00000611342.1:c.*803G>C	ENSP00000480366.1:n.*803G>C
NM_001934.3:c.*210G>C	NP_001925.2:n.*210G>C
NM_138281.2:c.*210G>C	NP_612138.1:n.*210G>C
XM_011524459.1:c.*210G>C	XP_011522761.1:n.*210G>C
XM_017024291.1:c.*210G>C	XP_016879780.1:n.*210G>C
NM_138281.3:c.*210G>C MANE Select	NP_612138.1:n.*210G>C
NM_001934.4:c.*210G>C	NP_001925.2:n.*210G>C