Canonical Allele Identifier: CA476785629

Gene: DIXDC1

Linked Data

• gnomAD v4: 11-112016782-C-A
• MyVariant Identifiers: chr11:g.111887506C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112016782C>A , CM000673.2:g.112016782C>A	GRCh38
NC_000011.9:g.111887506C>A , CM000673.1:g.111887506C>A	GRCh37
NC_000011.8:g.111392716C>A	NCBI36
NG_033127.1:g.94640C>A
NG_033127.2:g.94639C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440460.7:c.1848C>A MANE Select	ENSP00000394352.3:p.Val616=
ENST00000440460.6:c.1848C>A	ENSP00000394352.3:p.Val616=
ENST00000526500.5:n.844C>A
ENST00000615255.1:c.1215C>A	ENSP00000480808.1:p.Val405=
ENST00000618522.4:n.1201C>A
NM_001037954.3:c.1848C>A	NP_001033043.1:p.Val616=
NM_033425.4:c.1215C>A	NP_219493.1:p.Val405=
XM_005277726.3:c.1848C>A	XP_005277783.1:p.Val616=
XM_005277727.3:c.1845C>A	XP_005277784.1:p.Val615=
XM_005277728.3:c.1215C>A	XP_005277785.1:p.Val405=
XM_011543045.1:c.966C>A	XP_011541347.1:p.Val322=
XM_011543046.1:c.960C>A	XP_011541348.1:p.Val320=
XM_017018466.2:c.1845C>A	XP_016873955.1:p.Val615=
XM_017018467.1:c.1845C>A	XP_016873956.1:p.Val615=
XM_017018468.1:c.966C>A	XP_016873957.1:p.Val322=
XM_017018469.1:c.960C>A	XP_016873958.1:p.Val320=
XM_024448742.1:c.1740C>A	XP_024304510.1:p.Val580=
XM_024448743.1:c.1737C>A	XP_024304511.1:p.Val579=
NM_001037954.4:c.1848C>A MANE Select	NP_001033043.1:p.Val616=
NM_033425.5:c.1215C>A	NP_219493.1:p.Val405=