Canonical Allele Identifier: CA2263813895
Gene: DLX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49973899_49973900delinsCA , CM000679.2:g.49973899_49973900delinsCA GRCh38
NC_000017.10:g.48051263_48051264delinsCA , CM000679.1:g.48051263_48051264delinsCA GRCh37
NC_000017.9:g.45406262_45406263delinsCA NCBI36
NG_030592.1:g.9702_9703delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000706528.1:n.1560_1561delinsCA
ENST00000240306.5:c.679_680delinsCA MANE Select ENSP00000240306.3:p.Gln227=
ENST00000240306.4:c.679_680delinsCA ENSP00000240306.3:p.Gln227=
ENST00000411890.3:c.463_464delinsCA ENSP00000410622.2:p.Gln155=
ENST00000611342.1:c.*549_*550delinsCA ENSP00000480366.1:n.*549_*550delinsCA
NM_001934.3:c.463_464delinsCA NP_001925.2:p.Gln155=
NM_138281.2:c.679_680delinsCA NP_612138.1:p.Gln227=
XM_011524459.1:c.463_464delinsCA XP_011522761.1:p.Gln155=
XM_017024291.1:c.463_464delinsCA XP_016879780.1:p.Gln155=
NM_138281.3:c.679_680delinsCA MANE Select NP_612138.1:p.Gln227=
NM_001934.4:c.463_464delinsCA NP_001925.2:p.Gln155=