Canonical Allele Identifier: CA671773712

Gene: DIXDC1

Linked Data

• dbSNP Id: rs1467529756
• MyVariant Identifiers: chr11:g.112016961_112016962insACT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112016963_112016965dup , CM000673.2:g.112016963_112016965dup	GRCh38
NC_000011.9:g.111887687_111887689dup , CM000673.1:g.111887687_111887689dup	GRCh37
NC_000011.8:g.111392897_111392899dup	NCBI36
NG_033127.1:g.94821_94823dup
NG_033127.2:g.94820_94822dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440460.7:c.1862+167_1862+169dup MANE Select	ENSP00000394352.3:n.1862+167_1862+169dup
ENST00000440460.6:c.1862+167_1862+169dup	ENSP00000394352.3:n.1862+167_1862+169dup
ENST00000526500.5:n.858+167_858+169dup
ENST00000615255.1:c.1229+167_1229+169dup	ENSP00000480808.1:n.1229+167_1229+169dup
ENST00000618522.4:n.1215+167_1215+169dup
NM_001037954.3:c.1862+167_1862+169dup	NP_001033043.1:n.1862+167_1862+169dup
NM_033425.4:c.1229+167_1229+169dup	NP_219493.1:n.1229+167_1229+169dup
XM_005277726.3:c.1862+167_1862+169dup	XP_005277783.1:n.1862+167_1862+169dup
XM_005277727.3:c.1859+167_1859+169dup	XP_005277784.1:n.1859+167_1859+169dup
XM_005277728.3:c.1229+167_1229+169dup	XP_005277785.1:n.1229+167_1229+169dup
XM_011543045.1:c.980+167_980+169dup	XP_011541347.1:n.980+167_980+169dup
XM_011543046.1:c.974+167_974+169dup	XP_011541348.1:n.974+167_974+169dup
XM_017018466.2:c.1859+167_1859+169dup	XP_016873955.1:n.1859+167_1859+169dup
XM_017018467.1:c.1859+167_1859+169dup	XP_016873956.1:n.1859+167_1859+169dup
XM_017018468.1:c.980+167_980+169dup	XP_016873957.1:n.980+167_980+169dup
XM_017018469.1:c.974+167_974+169dup	XP_016873958.1:n.974+167_974+169dup
XM_024448742.1:c.1754+167_1754+169dup	XP_024304510.1:n.1754+167_1754+169dup
XM_024448743.1:c.1751+167_1751+169dup	XP_024304511.1:n.1751+167_1751+169dup
NM_001037954.4:c.1862+167_1862+169dup MANE Select	NP_001033043.1:n.1862+167_1862+169dup
NM_033425.5:c.1229+167_1229+169dup	NP_219493.1:n.1229+167_1229+169dup