Canonical Allele Identifier: CA2638666326

Gene: DLX4

Linked Data

• gnomAD v4: 17-49974119-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49974119G>T , CM000679.2:g.49974119G>T	GRCh38
NC_000017.10:g.48051483G>T , CM000679.1:g.48051483G>T	GRCh37
NC_000017.9:g.45406482G>T	NCBI36
NG_030592.1:g.9922G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706528.1:n.1780G>T
ENST00000240306.5:c.*176G>T MANE Select	ENSP00000240306.3:n.*176G>T
ENST00000240306.4:c.*176G>T	ENSP00000240306.3:n.*176G>T
ENST00000411890.3:c.*176G>T	ENSP00000410622.2:n.*176G>T
ENST00000611342.1:c.*769G>T	ENSP00000480366.1:n.*769G>T
NM_001934.3:c.*176G>T	NP_001925.2:n.*176G>T
NM_138281.2:c.*176G>T	NP_612138.1:n.*176G>T
XM_011524459.1:c.*176G>T	XP_011522761.1:n.*176G>T
XM_017024291.1:c.*176G>T	XP_016879780.1:n.*176G>T
NM_138281.3:c.*176G>T MANE Select	NP_612138.1:n.*176G>T
NM_001934.4:c.*176G>T	NP_001925.2:n.*176G>T