Canonical Allele Identifier: CA2263813924
Gene: DLX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49973957_49973958delinsCG , CM000679.2:g.49973957_49973958delinsCG GRCh38
NC_000017.10:g.48051321_48051322delinsCG , CM000679.1:g.48051321_48051322delinsCG GRCh37
NC_000017.9:g.45406320_45406321delinsCG NCBI36
NG_030592.1:g.9760_9761delinsCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000706528.1:n.1618_1619delinsCG
ENST00000240306.5:c.*14_*15delinsCG MANE Select ENSP00000240306.3:n.*14_*15delinsCG
ENST00000240306.4:c.*14_*15delinsCG ENSP00000240306.3:n.*14_*15delinsCG
ENST00000411890.3:c.*14_*15delinsCG ENSP00000410622.2:n.*14_*15delinsCG
ENST00000611342.1:c.*607_*608delinsCG ENSP00000480366.1:n.*607_*608delinsCG
NM_001934.3:c.*14_*15delinsCG NP_001925.2:n.*14_*15delinsCG
NM_138281.2:c.*14_*15delinsCG NP_612138.1:n.*14_*15delinsCG
XM_011524459.1:c.*14_*15delinsCG XP_011522761.1:n.*14_*15delinsCG
XM_017024291.1:c.*14_*15delinsCG XP_016879780.1:n.*14_*15delinsCG
NM_138281.3:c.*14_*15delinsCG MANE Select NP_612138.1:n.*14_*15delinsCG
NM_001934.4:c.*14_*15delinsCG NP_001925.2:n.*14_*15delinsCG