Canonical Allele Identifier: CA2263813863
Gene: DLX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49973831_49973833delinsTCT , CM000679.2:g.49973831_49973833delinsTCT GRCh38
NC_000017.10:g.48051195_48051197delinsTCT , CM000679.1:g.48051195_48051197delinsTCT GRCh37
NC_000017.9:g.45406194_45406196delinsTCT NCBI36
NG_030592.1:g.9634_9636delinsTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000706528.1:n.1492_1494delinsTCT
ENST00000240306.5:c.611_613delinsTCT MANE Select ENSP00000240306.3:p.Leu204=
ENST00000240306.4:c.611_613delinsTCT ENSP00000240306.3:p.Leu204=
ENST00000411890.3:c.395_397delinsTCT ENSP00000410622.2:p.Leu132=
ENST00000611342.1:c.*481_*483delinsTCT ENSP00000480366.1:n.*481_*483delinsTCT
NM_001934.3:c.395_397delinsTCT NP_001925.2:p.Leu132=
NM_138281.2:c.611_613delinsTCT NP_612138.1:p.Leu204=
XM_011524459.1:c.395_397delinsTCT XP_011522761.1:p.Leu132=
XM_017024291.1:c.395_397delinsTCT XP_016879780.1:p.Leu132=
NM_138281.3:c.611_613delinsTCT MANE Select NP_612138.1:p.Leu204=
NM_001934.4:c.395_397delinsTCT NP_001925.2:p.Leu132=