Canonical Allele Identifier: CA2000524038
Gene: DIXDC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112016693T= , CM000673.2:g.112016693T= GRCh38
NC_000011.9:g.111887417T= , CM000673.1:g.111887417T= GRCh37
NC_000011.8:g.111392627T= NCBI36
NG_033127.1:g.94551T=
NG_033127.2:g.94550T=

Transcript Alleles

HGVS Amino-acid change
ENST00000440460.7:c.1759T= MANE Select ENSP00000394352.3:p.Leu587=
ENST00000440460.6:c.1759T= ENSP00000394352.3:p.Leu587=
ENST00000526500.5:n.755T=
ENST00000615255.1:c.1126T= ENSP00000480808.1:p.Leu376=
ENST00000618522.4:n.1112T=
NM_001037954.3:c.1759T= NP_001033043.1:p.Leu587=
NM_033425.4:c.1126T= NP_219493.1:p.Leu376=
XM_005277726.3:c.1759T= XP_005277783.1:p.Leu587=
XM_005277727.3:c.1756T= XP_005277784.1:p.Leu586=
XM_005277728.3:c.1126T= XP_005277785.1:p.Leu376=
XM_011543045.1:c.877T= XP_011541347.1:p.Leu293=
XM_011543046.1:c.871T= XP_011541348.1:p.Leu291=
XM_017018466.2:c.1756T= XP_016873955.1:p.Leu586=
XM_017018467.1:c.1756T= XP_016873956.1:p.Leu586=
XM_017018468.1:c.877T= XP_016873957.1:p.Leu293=
XM_017018469.1:c.871T= XP_016873958.1:p.Leu291=
XM_024448742.1:c.1651T= XP_024304510.1:p.Leu551=
XM_024448743.1:c.1648T= XP_024304511.1:p.Leu550=
NM_001037954.4:c.1759T= MANE Select NP_001033043.1:p.Leu587=
NM_033425.5:c.1126T= NP_219493.1:p.Leu376=