Canonical Allele Identifier: CA2263813995
Gene: DLX4 HGNC NCBI

Linked Data

dbSNP Id: rs1905632546

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49974120C>G , CM000679.2:g.49974120C>G GRCh38
NC_000017.10:g.48051484C>G , CM000679.1:g.48051484C>G GRCh37
NC_000017.9:g.45406483C>G NCBI36
NG_030592.1:g.9923C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000706528.1:n.1781C>G
ENST00000240306.5:c.*177C>G MANE Select ENSP00000240306.3:n.*177C>G
ENST00000240306.4:c.*177C>G ENSP00000240306.3:n.*177C>G
ENST00000411890.3:c.*177C>G ENSP00000410622.2:n.*177C>G
ENST00000611342.1:c.*770C>G ENSP00000480366.1:n.*770C>G
NM_001934.3:c.*177C>G NP_001925.2:n.*177C>G
NM_138281.2:c.*177C>G NP_612138.1:n.*177C>G
XM_011524459.1:c.*177C>G XP_011522761.1:n.*177C>G
XM_017024291.1:c.*177C>G XP_016879780.1:n.*177C>G
NM_138281.3:c.*177C>G MANE Select NP_612138.1:n.*177C>G
NM_001934.4:c.*177C>G NP_001925.2:n.*177C>G