Canonical Allele Identifier: CA382589852

Gene: DIXDC1

Linked Data

• gnomAD v4: 11-112016699-C-G
• MyVariant Identifiers: chr11:g.111887423C>G (hg19) ; chr11:g.112016699C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112016699C>G , CM000673.2:g.112016699C>G	GRCh38
NC_000011.9:g.111887423C>G , CM000673.1:g.111887423C>G	GRCh37
NC_000011.8:g.111392633C>G	NCBI36
NG_033127.1:g.94557C>G
NG_033127.2:g.94556C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440460.7:c.1765C>G MANE Select	ENSP00000394352.3:p.His589Asp
ENST00000440460.6:c.1765C>G	ENSP00000394352.3:p.His589Asp
ENST00000526500.5:n.761C>G
ENST00000615255.1:c.1132C>G	ENSP00000480808.1:p.His378Asp
ENST00000618522.4:n.1118C>G
NM_001037954.3:c.1765C>G	NP_001033043.1:p.His589Asp
NM_033425.4:c.1132C>G	NP_219493.1:p.His378Asp
XM_005277726.3:c.1765C>G	XP_005277783.1:p.His589Asp
XM_005277727.3:c.1762C>G	XP_005277784.1:p.His588Asp
XM_005277728.3:c.1132C>G	XP_005277785.1:p.His378Asp
XM_011543045.1:c.883C>G	XP_011541347.1:p.His295Asp
XM_011543046.1:c.877C>G	XP_011541348.1:p.His293Asp
XM_017018466.2:c.1762C>G	XP_016873955.1:p.His588Asp
XM_017018467.1:c.1762C>G	XP_016873956.1:p.His588Asp
XM_017018468.1:c.883C>G	XP_016873957.1:p.His295Asp
XM_017018469.1:c.877C>G	XP_016873958.1:p.His293Asp
XM_024448742.1:c.1657C>G	XP_024304510.1:p.His553Asp
XM_024448743.1:c.1654C>G	XP_024304511.1:p.His552Asp
NM_001037954.4:c.1765C>G MANE Select	NP_001033043.1:p.His589Asp
NM_033425.5:c.1132C>G	NP_219493.1:p.His378Asp