Canonical Allele Identifier: CA2695205730

Gene: NSD1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177282510_177282512del , CM000667.2:g.177282510_177282512del	GRCh38
NC_000005.9:g.176709511_176709513del , CM000667.1:g.176709511_176709513del	GRCh37
NC_000005.8:g.176642117_176642119del	NCBI36
NG_009821.1:g.154432_154434del , LRG_512:g.154432_154434del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508896.7:c.5065_5067del	ENSP00000423372.3:p.Glu1689del
ENST00000347982.9:c.5065_5067del	ENSP00000343209.5:p.Glu1689del
ENST00000354179.9:c.5065_5067del	ENSP00000346111.5:p.Glu1689del
ENST00000503056.6:c.580_582del	ENSP00000424024.2:p.Glu194del
ENST00000508029.6:c.580_582del	ENSP00000425120.2:p.Glu194del
ENST00000685206.1:n.5521_5523del
ENST00000686993.1:c.5065_5067del	ENSP00000510020.1:p.Glu1689del
ENST00000687453.1:c.5629_5631del	ENSP00000508426.1:p.Glu1877del
ENST00000688613.1:n.5335_5337del
ENST00000689345.1:c.5065_5067del	ENSP00000509711.1:p.Glu1689del
ENST00000689549.1:n.6085_6087del
ENST00000692024.1:n.4487_4489del
ENST00000439151.7:c.5938_5940del MANE Select	ENSP00000395929.2:p.Glu1980del
ENST00000347982.8:c.5131_5133del	ENSP00000343209.4:p.Glu1711del
ENST00000354179.8:c.5131_5133del	ENSP00000346111.4:p.Glu1711del
ENST00000439151.6:c.5938_5940del	ENSP00000395929.2:p.Glu1980del
NM_022455.4:c.5938_5940del , LRG_512t1:c.5938_5940del	NP_071900.2:p.Glu1980del
NM_172349.2:c.5131_5133del	NP_758859.1:p.Glu1711del
XM_005265959.1:c.5938_5940del	XP_005266016.1:p.Glu1980del
XM_005265960.1:c.5131_5133del	XP_005266017.1:p.Glu1711del
XM_005265961.1:c.5131_5133del	XP_005266018.1:p.Glu1711del
XM_005265962.3:c.1432_1434del	XP_005266019.1:p.Glu478del
XM_011534610.1:c.5938_5940del	XP_011532912.1:p.Glu1980del
XM_011534611.1:c.5938_5940del	XP_011532913.1:p.Glu1980del
XM_011534612.1:c.5518_5520del	XP_011532914.1:p.Glu1840del
XM_011534613.1:c.4882_4884del	XP_011532915.1:p.Glu1628del
XM_011534617.1:c.1672_1674del	XP_011532919.1:p.Glu558del
NM_001365684.1:c.5131_5133del	NP_001352613.1:p.Glu1711del
XM_024446150.1:c.5938_5940del	XP_024301918.1:p.Glu1980del
XM_024446151.1:c.5938_5940del	XP_024301919.1:p.Glu1980del
XM_024446152.1:c.5938_5940del	XP_024301920.1:p.Glu1980del
XM_024446153.1:c.5938_5940del	XP_024301921.1:p.Glu1980del
XM_024446154.1:c.5518_5520del	XP_024301922.1:p.Glu1840del
XM_024446155.1:c.5131_5133del	XP_024301923.1:p.Glu1711del
XM_024446156.1:c.5131_5133del	XP_024301924.1:p.Glu1711del
XM_024446158.1:c.5131_5133del	XP_024301926.1:p.Glu1711del
XM_024446159.1:c.4882_4884del	XP_024301927.1:p.Glu1628del
XM_024446162.1:c.1672_1674del	XP_024301930.1:p.Glu558del
XM_024446163.1:c.1432_1434del	XP_024301931.1:p.Glu478del
NM_022455.5:c.5938_5940del MANE Select	NP_071900.2:p.Glu1980del
NM_172349.3:c.5131_5133del	NP_758859.1:p.Glu1711del