Canonical Allele Identifier: CA2638666346
Gene: DLX4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49974132C>A , CM000679.2:g.49974132C>A GRCh38
NC_000017.10:g.48051496C>A , CM000679.1:g.48051496C>A GRCh37
NC_000017.9:g.45406495C>A NCBI36
NG_030592.1:g.9935C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000706528.1:n.1793C>A
ENST00000240306.5:c.*189C>A MANE Select ENSP00000240306.3:n.*189C>A
ENST00000240306.4:c.*189C>A ENSP00000240306.3:n.*189C>A
ENST00000411890.3:c.*189C>A ENSP00000410622.2:n.*189C>A
ENST00000611342.1:c.*782C>A ENSP00000480366.1:n.*782C>A
NM_001934.3:c.*189C>A NP_001925.2:n.*189C>A
NM_138281.2:c.*189C>A NP_612138.1:n.*189C>A
XM_011524459.1:c.*189C>A XP_011522761.1:n.*189C>A
XM_017024291.1:c.*189C>A XP_016879780.1:n.*189C>A
NM_138281.3:c.*189C>A MANE Select NP_612138.1:n.*189C>A
NM_001934.4:c.*189C>A NP_001925.2:n.*189C>A