Canonical Allele Identifier: CA2263814032
Gene: DLX4 HGNC NCBI

Linked Data

dbSNP Id: rs1598148880

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49974228A>G , CM000679.2:g.49974228A>G GRCh38
NC_000017.10:g.48051592A>G , CM000679.1:g.48051592A>G GRCh37
NC_000017.9:g.45406591A>G NCBI36
NG_030592.1:g.10031A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000706528.1:n.1889A>G
ENST00000240306.5:c.*285A>G MANE Select ENSP00000240306.3:n.*285A>G
ENST00000240306.4:c.*285A>G ENSP00000240306.3:n.*285A>G
ENST00000411890.3:c.*285A>G ENSP00000410622.2:n.*285A>G
ENST00000611342.1:c.*878A>G ENSP00000480366.1:n.*878A>G
NM_001934.3:c.*285A>G NP_001925.2:n.*285A>G
NM_138281.2:c.*285A>G NP_612138.1:n.*285A>G
XM_011524459.1:c.*285A>G XP_011522761.1:n.*285A>G
XM_017024291.1:c.*285A>G XP_016879780.1:n.*285A>G
NM_138281.3:c.*285A>G MANE Select NP_612138.1:n.*285A>G
NM_001934.4:c.*285A>G NP_001925.2:n.*285A>G