Canonical Allele Identifier: CA2000524039

Gene: DIXDC1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112016697C= , CM000673.2:g.112016697C=	GRCh38
NC_000011.9:g.111887421C= , CM000673.1:g.111887421C=	GRCh37
NC_000011.8:g.111392631C=	NCBI36
NG_033127.1:g.94555C=
NG_033127.2:g.94554C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440460.7:c.1763C= MANE Select	ENSP00000394352.3:p.Pro588=
ENST00000440460.6:c.1763C=	ENSP00000394352.3:p.Pro588=
ENST00000526500.5:n.759C=
ENST00000615255.1:c.1130C=	ENSP00000480808.1:p.Pro377=
ENST00000618522.4:n.1116C=
NM_001037954.3:c.1763C=	NP_001033043.1:p.Pro588=
NM_033425.4:c.1130C=	NP_219493.1:p.Pro377=
XM_005277726.3:c.1763C=	XP_005277783.1:p.Pro588=
XM_005277727.3:c.1760C=	XP_005277784.1:p.Pro587=
XM_005277728.3:c.1130C=	XP_005277785.1:p.Pro377=
XM_011543045.1:c.881C=	XP_011541347.1:p.Pro294=
XM_011543046.1:c.875C=	XP_011541348.1:p.Pro292=
XM_017018466.2:c.1760C=	XP_016873955.1:p.Pro587=
XM_017018467.1:c.1760C=	XP_016873956.1:p.Pro587=
XM_017018468.1:c.881C=	XP_016873957.1:p.Pro294=
XM_017018469.1:c.875C=	XP_016873958.1:p.Pro292=
XM_024448742.1:c.1655C=	XP_024304510.1:p.Pro552=
XM_024448743.1:c.1652C=	XP_024304511.1:p.Pro551=
NM_001037954.4:c.1763C= MANE Select	NP_001033043.1:p.Pro588=
NM_033425.5:c.1130C=	NP_219493.1:p.Pro377=