Canonical Allele Identifier: CA2809765333

Gene: DLX4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49973826_49973827insACCCAC , CM000679.2:g.49973826_49973827insACCCAC	GRCh38
NC_000017.10:g.48051190_48051191insACCCAC , CM000679.1:g.48051190_48051191insACCCAC	GRCh37
NC_000017.9:g.45406189_45406190insACCCAC	NCBI36
NG_030592.1:g.9629_9630insACCCAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706528.1:n.1487_1488insACCCAC
ENST00000240306.5:c.606_607insACCCAC MANE Select	ENSP00000240306.3:p.Pro202_Ser203insThrHis
ENST00000240306.4:c.606_607insACCCAC	ENSP00000240306.3:p.Pro202_Ser203insThrHis
ENST00000411890.3:c.390_391insACCCAC	ENSP00000410622.2:p.Pro130_Ser131insThrHis
ENST00000611342.1:c.*476_*477insACCCAC	ENSP00000480366.1:n.*476_*477insACCCAC
NM_001934.3:c.390_391insACCCAC	NP_001925.2:p.Pro130_Ser131insThrHis
NM_138281.2:c.606_607insACCCAC	NP_612138.1:p.Pro202_Ser203insThrHis
XM_011524459.1:c.390_391insACCCAC	XP_011522761.1:p.Pro130_Ser131insThrHis
XM_017024291.1:c.390_391insACCCAC	XP_016879780.1:p.Pro130_Ser131insThrHis
NM_138281.3:c.606_607insACCCAC MANE Select	NP_612138.1:p.Pro202_Ser203insThrHis
NM_001934.4:c.390_391insACCCAC	NP_001925.2:p.Pro130_Ser131insThrHis