Canonical Allele Identifier: CA2000524068

Gene: DIXDC1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112016777A= , CM000673.2:g.112016777A=	GRCh38
NC_000011.9:g.111887501A= , CM000673.1:g.111887501A=	GRCh37
NC_000011.8:g.111392711A=	NCBI36
NG_033127.1:g.94635A=
NG_033127.2:g.94634A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440460.7:c.1843A= MANE Select	ENSP00000394352.3:p.Met615=
ENST00000440460.6:c.1843A=	ENSP00000394352.3:p.Met615=
ENST00000526500.5:n.839A=
ENST00000615255.1:c.1210A=	ENSP00000480808.1:p.Met404=
ENST00000618522.4:n.1196A=
NM_001037954.3:c.1843A=	NP_001033043.1:p.Met615=
NM_033425.4:c.1210A=	NP_219493.1:p.Met404=
XM_005277726.3:c.1843A=	XP_005277783.1:p.Met615=
XM_005277727.3:c.1840A=	XP_005277784.1:p.Met614=
XM_005277728.3:c.1210A=	XP_005277785.1:p.Met404=
XM_011543045.1:c.961A=	XP_011541347.1:p.Met321=
XM_011543046.1:c.955A=	XP_011541348.1:p.Met319=
XM_017018466.2:c.1840A=	XP_016873955.1:p.Met614=
XM_017018467.1:c.1840A=	XP_016873956.1:p.Met614=
XM_017018468.1:c.961A=	XP_016873957.1:p.Met321=
XM_017018469.1:c.955A=	XP_016873958.1:p.Met319=
XM_024448742.1:c.1735A=	XP_024304510.1:p.Met579=
XM_024448743.1:c.1732A=	XP_024304511.1:p.Met578=
NM_001037954.4:c.1843A= MANE Select	NP_001033043.1:p.Met615=
NM_033425.5:c.1210A=	NP_219493.1:p.Met404=