Canonical Allele Identifier: CA400168588
Gene: DLX4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.49973855C>A , CM000679.2:g.49973855C>A GRCh38
NC_000017.10:g.48051219C>A , CM000679.1:g.48051219C>A GRCh37
NC_000017.9:g.45406218C>A NCBI36
NG_030592.1:g.9658C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000706528.1:n.1516C>A
ENST00000240306.5:c.635C>A MANE Select ENSP00000240306.3:p.Thr212Asn
ENST00000240306.4:c.635C>A ENSP00000240306.3:p.Thr212Asn
ENST00000411890.3:c.419C>A ENSP00000410622.2:p.Thr140Asn
ENST00000611342.1:c.*505C>A ENSP00000480366.1:n.*505C>A
NM_001934.3:c.419C>A NP_001925.2:p.Thr140Asn
NM_138281.2:c.635C>A NP_612138.1:p.Thr212Asn
XM_011524459.1:c.419C>A XP_011522761.1:p.Thr140Asn
XM_017024291.1:c.419C>A XP_016879780.1:p.Thr140Asn
NM_138281.3:c.635C>A MANE Select NP_612138.1:p.Thr212Asn
NM_001934.4:c.419C>A NP_001925.2:p.Thr140Asn