Canonical Allele Identifier: CA2263813874
Gene: DLX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49973847_49973854delinsGGCAGGGA , CM000679.2:g.49973847_49973854delinsGGCAGGGA GRCh38
NC_000017.10:g.48051211_48051218delinsGGCAGGGA , CM000679.1:g.48051211_48051218delinsGGCAGGGA GRCh37
NC_000017.9:g.45406210_45406217delinsGGCAGGGA NCBI36
NG_030592.1:g.9650_9657delinsGGCAGGGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000706528.1:n.1508_1515delinsGGCAGGGA
ENST00000240306.5:c.627_634delinsGGCAGGGA MANE Select ENSP00000240306.3:p.Lys209=
ENST00000240306.4:c.627_634delinsGGCAGGGA ENSP00000240306.3:p.Lys209=
ENST00000411890.3:c.411_418delinsGGCAGGGA ENSP00000410622.2:p.Lys137=
ENST00000611342.1:c.*497_*504delinsGGCAGGGA ENSP00000480366.1:n.*497_*504delinsGGCAGGGA
NM_001934.3:c.411_418delinsGGCAGGGA NP_001925.2:p.Lys137=
NM_138281.2:c.627_634delinsGGCAGGGA NP_612138.1:p.Lys209=
XM_011524459.1:c.411_418delinsGGCAGGGA XP_011522761.1:p.Lys137=
XM_017024291.1:c.411_418delinsGGCAGGGA XP_016879780.1:p.Lys137=
NM_138281.3:c.627_634delinsGGCAGGGA MANE Select NP_612138.1:p.Lys209=
NM_001934.4:c.411_418delinsGGCAGGGA NP_001925.2:p.Lys137=