Canonical Allele Identifier: CA2000524126

Gene: DIXDC1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.112016948_112016955delinsGTTTCAGC , CM000673.2:g.112016948_112016955delinsGTTTCAGC	GRCh38
NC_000011.9:g.111887672_111887679delinsGTTTCAGC , CM000673.1:g.111887672_111887679delinsGTTTCAGC	GRCh37
NC_000011.8:g.111392882_111392889delinsGTTTCAGC	NCBI36
NG_033127.1:g.94806_94813delinsGTTTCAGC
NG_033127.2:g.94805_94812delinsGTTTCAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440460.7:c.1862+152_1862+159delinsGTTTCAGC MANE Select	ENSP00000394352.3:n.1862+152_1862+159delinsGTTTCAGC
ENST00000440460.6:c.1862+152_1862+159delinsGTTTCAGC	ENSP00000394352.3:n.1862+152_1862+159delinsGTTTCAGC
ENST00000526500.5:n.858+152_858+159delinsGTTTCAGC
ENST00000615255.1:c.1229+152_1229+159delinsGTTTCAGC	ENSP00000480808.1:n.1229+152_1229+159delinsGTTTCAGC
ENST00000618522.4:n.1215+152_1215+159delinsGTTTCAGC
NM_001037954.3:c.1862+152_1862+159delinsGTTTCAGC	NP_001033043.1:n.1862+152_1862+159delinsGTTTCAGC
NM_033425.4:c.1229+152_1229+159delinsGTTTCAGC	NP_219493.1:n.1229+152_1229+159delinsGTTTCAGC
XM_005277726.3:c.1862+152_1862+159delinsGTTTCAGC	XP_005277783.1:n.1862+152_1862+159delinsGTTTCAGC
XM_005277727.3:c.1859+152_1859+159delinsGTTTCAGC	XP_005277784.1:n.1859+152_1859+159delinsGTTTCAGC
XM_005277728.3:c.1229+152_1229+159delinsGTTTCAGC	XP_005277785.1:n.1229+152_1229+159delinsGTTTCAGC
XM_011543045.1:c.980+152_980+159delinsGTTTCAGC	XP_011541347.1:n.980+152_980+159delinsGTTTCAGC
XM_011543046.1:c.974+152_974+159delinsGTTTCAGC	XP_011541348.1:n.974+152_974+159delinsGTTTCAGC
XM_017018466.2:c.1859+152_1859+159delinsGTTTCAGC	XP_016873955.1:n.1859+152_1859+159delinsGTTTCAGC
XM_017018467.1:c.1859+152_1859+159delinsGTTTCAGC	XP_016873956.1:n.1859+152_1859+159delinsGTTTCAGC
XM_017018468.1:c.980+152_980+159delinsGTTTCAGC	XP_016873957.1:n.980+152_980+159delinsGTTTCAGC
XM_017018469.1:c.974+152_974+159delinsGTTTCAGC	XP_016873958.1:n.974+152_974+159delinsGTTTCAGC
XM_024448742.1:c.1754+152_1754+159delinsGTTTCAGC	XP_024304510.1:n.1754+152_1754+159delinsGTTTCAGC
XM_024448743.1:c.1751+152_1751+159delinsGTTTCAGC	XP_024304511.1:n.1751+152_1751+159delinsGTTTCAGC
NM_001037954.4:c.1862+152_1862+159delinsGTTTCAGC MANE Select	NP_001033043.1:n.1862+152_1862+159delinsGTTTCAGC
NM_033425.5:c.1229+152_1229+159delinsGTTTCAGC	NP_219493.1:n.1229+152_1229+159delinsGTTTCAGC