Canonical Allele Identifier: CA621059101

Gene: NDE1

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.15665071del , CM000678.2:g.15665071del	GRCh38
NC_000016.9:g.15758928del , CM000678.1:g.15758928del	GRCh37
NC_000016.8:g.15666429del	NCBI36
NG_021210.1:g.26805del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396354.6:c.83+210del MANE Select	ENSP00000379642.1:n.83+210del
ENST00000572756.6:c.83+210del	ENSP00000460436.2:n.83+210del
ENST00000577101.6:c.83+210del	ENSP00000461729.2:n.83+210del
ENST00000674538.1:c.83+210del	ENSP00000501547.1:n.83+210del
ENST00000674554.1:c.83+210del	ENSP00000502635.1:n.83+210del
ENST00000674581.1:c.83+210del	ENSP00000502100.1:n.83+210del
ENST00000674588.1:c.83+210del	ENSP00000502802.1:n.83+210del
ENST00000674888.1:c.83+210del	ENSP00000501936.1:n.83+210del
ENST00000674900.1:c.83+210del	ENSP00000502662.1:n.83+210del
ENST00000674995.1:c.83+210del	ENSP00000502414.1:n.83+210del
ENST00000675171.1:c.83+210del	ENSP00000501812.1:n.83+210del
ENST00000675926.1:c.83+210del	ENSP00000502354.1:n.83+210del
ENST00000675951.1:c.83+210del	ENSP00000502160.1:n.83+210del
ENST00000342673.9:c.83+210del	ENSP00000345892.5:n.83+210del
ENST00000396354.5:c.83+210del	ENSP00000379642.1:n.83+210del
ENST00000396355.5:c.83+210del	ENSP00000379643.1:n.83+210del
ENST00000570727.5:c.83+210del	ENSP00000459889.1:n.83+210del
ENST00000572756.5:c.83+210del	ENSP00000460436.1:n.83+210del
ENST00000573203.5:c.83+210del	ENSP00000460996.1:n.83+210del
NM_001143979.1:c.83+210del	NP_001137451.1:n.83+210del
NM_017668.2:c.83+210del	NP_060138.1:n.83+210del
XM_005255396.3:c.83+210del	XP_005255453.1:n.83+210del
XM_006720897.2:c.179+210del	XP_006720960.1:n.179+210del
XM_006720898.2:c.179+210del	XP_006720961.1:n.179+210del
XM_006720899.2:c.179+210del	XP_006720962.1:n.179+210del
XM_006720900.2:c.83+210del	XP_006720963.1:n.83+210del
XM_011522549.1:c.179+210del	XP_011520851.1:n.179+210del
XM_011522550.1:c.179+210del	XP_011520852.1:n.179+210del
XM_011522551.1:c.179+210del	XP_011520853.1:n.179+210del
XM_011522552.1:c.179+210del	XP_011520854.1:n.179+210del
XM_011522553.1:c.83+210del	XP_011520855.1:n.83+210del
XM_011522554.1:c.179+210del	XP_011520856.1:n.179+210del
XM_005255396.5:c.83+210del	XP_005255453.1:n.83+210del
XM_006720897.4:c.179+210del	XP_006720960.1:n.179+210del
XM_006720900.4:c.83+210del	XP_006720963.1:n.83+210del
XM_011522553.2:c.83+210del	XP_011520855.1:n.83+210del
XM_017023349.2:c.83+210del	XP_016878838.1:n.83+210del
XM_017023350.1:c.83+210del	XP_016878839.1:n.83+210del
XM_017023351.2:c.83+210del	XP_016878840.1:n.83+210del
XM_017023352.2:c.83+210del	XP_016878841.1:n.83+210del
XM_017023353.2:c.83+210del	XP_016878842.1:n.83+210del
XM_017023354.2:c.83+210del	XP_016878843.1:n.83+210del
XM_017023355.2:c.83+210del	XP_016878844.1:n.83+210del
XM_017023356.2:c.83+210del	XP_016878845.1:n.83+210del
NM_017668.3:c.83+210del MANE Select	NP_060138.1:n.83+210del
NM_001143979.2:c.83+210del	NP_001137451.1:n.83+210del