Canonical Allele Identifier: CA2263814018

Gene: DLX4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49974180_49974183delinsCCTT , CM000679.2:g.49974180_49974183delinsCCTT	GRCh38
NC_000017.10:g.48051544_48051547delinsCCTT , CM000679.1:g.48051544_48051547delinsCCTT	GRCh37
NC_000017.9:g.45406543_45406546delinsCCTT	NCBI36
NG_030592.1:g.9983_9986delinsCCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706528.1:n.1841_1844delinsCCTT
ENST00000240306.5:c.*237_*240delinsCCTT MANE Select	ENSP00000240306.3:n.*237_*240delinsCCTT
ENST00000240306.4:c.*237_*240delinsCCTT	ENSP00000240306.3:n.*237_*240delinsCCTT
ENST00000411890.3:c.*237_*240delinsCCTT	ENSP00000410622.2:n.*237_*240delinsCCTT
ENST00000611342.1:c.*830_*833delinsCCTT	ENSP00000480366.1:n.*830_*833delinsCCTT
NM_001934.3:c.*237_*240delinsCCTT	NP_001925.2:n.*237_*240delinsCCTT
NM_138281.2:c.*237_*240delinsCCTT	NP_612138.1:n.*237_*240delinsCCTT
XM_011524459.1:c.*237_*240delinsCCTT	XP_011522761.1:n.*237_*240delinsCCTT
XM_017024291.1:c.*237_*240delinsCCTT	XP_016879780.1:n.*237_*240delinsCCTT
NM_138281.3:c.*237_*240delinsCCTT MANE Select	NP_612138.1:n.*237_*240delinsCCTT
NM_001934.4:c.*237_*240delinsCCTT	NP_001925.2:n.*237_*240delinsCCTT