Canonical Allele Identifier: CA6017130
Gene: DTX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.59189190G>A , CM000673.2:g.59189190G>A GRCh38
NC_000011.9:g.58956663G>A , CM000673.1:g.58956663G>A GRCh37
NC_000011.8:g.58713239G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000227451.4:c.1026G>A MANE Select ENSP00000227451.3:p.Ala342=
ENST00000227451.3:c.1026G>A ENSP00000227451.3:p.Ala342=
ENST00000531902.1:n.145G>A
ENST00000532982.5:c.708G>A ENSP00000434055.1:p.Ala236=
NM_001300727.1:c.708G>A NP_001287656.1:p.Ala236=
NM_015177.1:c.1026G>A NP_055992.1:p.Ala342=
XM_006718483.2:c.708G>A XP_006718546.1:p.Ala236=
XM_006718483.3:c.708G>A XP_006718546.1:p.Ala236=
NM_015177.2:c.1026G>A MANE Select NP_055992.1:p.Ala342=
NM_001300727.2:c.708G>A NP_001287656.1:p.Ala236=