Canonical Allele Identifier: CA2638666492
Gene: DLX4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49974202A>G , CM000679.2:g.49974202A>G GRCh38
NC_000017.10:g.48051566A>G , CM000679.1:g.48051566A>G GRCh37
NC_000017.9:g.45406565A>G NCBI36
NG_030592.1:g.10005A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000706528.1:n.1863A>G
ENST00000240306.5:c.*259A>G MANE Select ENSP00000240306.3:n.*259A>G
ENST00000240306.4:c.*259A>G ENSP00000240306.3:n.*259A>G
ENST00000411890.3:c.*259A>G ENSP00000410622.2:n.*259A>G
ENST00000611342.1:c.*852A>G ENSP00000480366.1:n.*852A>G
NM_001934.3:c.*259A>G NP_001925.2:n.*259A>G
NM_138281.2:c.*259A>G NP_612138.1:n.*259A>G
XM_011524459.1:c.*259A>G XP_011522761.1:n.*259A>G
XM_017024291.1:c.*259A>G XP_016879780.1:n.*259A>G
NM_138281.3:c.*259A>G MANE Select NP_612138.1:n.*259A>G
NM_001934.4:c.*259A>G NP_001925.2:n.*259A>G