Canonical Allele Identifier: CA2638666568

Gene: DLX4

Linked Data

• gnomAD v4: 17-49974254-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49974254G>T , CM000679.2:g.49974254G>T	GRCh38
NC_000017.10:g.48051618G>T , CM000679.1:g.48051618G>T	GRCh37
NC_000017.9:g.45406617G>T	NCBI36
NG_030592.1:g.10057G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706528.1:n.1915G>T
ENST00000240306.5:c.*311G>T MANE Select	ENSP00000240306.3:n.*311G>T
ENST00000240306.4:c.*311G>T	ENSP00000240306.3:n.*311G>T
ENST00000411890.3:c.*311G>T	ENSP00000410622.2:n.*311G>T
ENST00000611342.1:c.*904G>T	ENSP00000480366.1:n.*904G>T
NM_001934.3:c.*311G>T	NP_001925.2:n.*311G>T
NM_138281.2:c.*311G>T	NP_612138.1:n.*311G>T
XM_011524459.1:c.*311G>T	XP_011522761.1:n.*311G>T
XM_017024291.1:c.*311G>T	XP_016879780.1:n.*311G>T
NM_138281.3:c.*311G>T MANE Select	NP_612138.1:n.*311G>T
NM_001934.4:c.*311G>T	NP_001925.2:n.*311G>T