Canonical Allele Identifier: CA2581314922
Gene: DLX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49974408C>A , CM000679.2:g.49974408C>A GRCh38
NC_000017.10:g.48051772C>A , CM000679.1:g.48051772C>A GRCh37
NC_000017.9:g.45406771C>A NCBI36
NG_030592.1:g.10211C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000706528.1:n.2069C>A
ENST00000240306.5:c.*465C>A MANE Select ENSP00000240306.3:n.*465C>A
ENST00000240306.4:c.*465C>A ENSP00000240306.3:n.*465C>A
ENST00000411890.3:c.*465C>A ENSP00000410622.2:n.*465C>A
ENST00000611342.1:c.*1058C>A ENSP00000480366.1:n.*1058C>A
NM_001934.3:c.*465C>A NP_001925.2:n.*465C>A
NM_138281.2:c.*465C>A NP_612138.1:n.*465C>A
XM_011524459.1:c.*465C>A XP_011522761.1:n.*465C>A
XM_017024291.1:c.*465C>A XP_016879780.1:n.*465C>A
NM_138281.3:c.*465C>A MANE Select NP_612138.1:n.*465C>A
NM_001934.4:c.*465C>A NP_001925.2:n.*465C>A