Canonical Allele Identifier: CA772784213

Gene: DLX4

Linked Data

• dbSNP Id: rs1050532650
• gnomAD v4: 17-49974180-C-A
• MyVariant Identifiers: chr17:g.48051544C>A (hg19) ; chr17:g.49974180C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49974180C>A , CM000679.2:g.49974180C>A	GRCh38
NC_000017.10:g.48051544C>A , CM000679.1:g.48051544C>A	GRCh37
NC_000017.9:g.45406543C>A	NCBI36
NG_030592.1:g.9983C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706528.1:n.1841C>A
ENST00000240306.5:c.*237C>A MANE Select	ENSP00000240306.3:n.*237C>A
ENST00000240306.4:c.*237C>A	ENSP00000240306.3:n.*237C>A
ENST00000411890.3:c.*237C>A	ENSP00000410622.2:n.*237C>A
ENST00000611342.1:c.*830C>A	ENSP00000480366.1:n.*830C>A
NM_001934.3:c.*237C>A	NP_001925.2:n.*237C>A
NM_138281.2:c.*237C>A	NP_612138.1:n.*237C>A
XM_011524459.1:c.*237C>A	XP_011522761.1:n.*237C>A
XM_017024291.1:c.*237C>A	XP_016879780.1:n.*237C>A
NM_138281.3:c.*237C>A MANE Select	NP_612138.1:n.*237C>A
NM_001934.4:c.*237C>A	NP_001925.2:n.*237C>A