Canonical Allele Identifier: CA645548641

Gene: NSD1

Linked Data

• COSMIC: COSM5982059 ; COSM5982060

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177282576_177282587del , CM000667.2:g.177282576_177282587del	GRCh38
NC_000005.9:g.176709577_176709588del , CM000667.1:g.176709577_176709588del	GRCh37
NC_000005.8:g.176642183_176642194del	NCBI36
NG_009821.1:g.154498_154509del , LRG_512:g.154498_154509del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508896.7:c.5131_5136+6del
ENST00000347982.9:c.5131_5136+6del
ENST00000354179.9:c.5131_5136+6del
ENST00000503056.6:c.646_651+6del
ENST00000508029.6:c.646_651+6del
ENST00000685206.1:n.5587_5592+6del
ENST00000686993.1:c.5131_5136+6del
ENST00000687453.1:c.5695_5700+6del
ENST00000688613.1:n.5401_5406+6del
ENST00000689345.1:c.5131_5136+6del
ENST00000689549.1:n.6151_6156+6del
ENST00000692024.1:n.4553_4558+6del
ENST00000439151.7:c.6004_6009+6del
ENST00000347982.8:c.5197_5202+6del
ENST00000354179.8:c.5197_5202+6del
ENST00000439151.6:c.6004_6009+6del
NM_022455.4:c.6004_6009+6del , LRG_512t1:c.6004_6009+6del
NM_172349.2:c.5197_5202+6del
XM_005265959.1:c.6004_6009+6del
XM_005265960.1:c.5197_5202+6del
XM_005265961.1:c.5197_5202+6del
XM_005265962.3:c.1498_1503+6del
XM_011534610.1:c.6004_6009+6del
XM_011534611.1:c.6004_6009+6del
XM_011534612.1:c.5584_5589+6del
XM_011534613.1:c.4948_4953+6del
XM_011534617.1:c.1738_1743+6del
NM_001365684.1:c.5197_5202+6del
XM_024446150.1:c.6004_6009+6del
XM_024446151.1:c.6004_6009+6del
XM_024446152.1:c.6004_6009+6del
XM_024446153.1:c.6004_6009+6del
XM_024446154.1:c.5584_5589+6del
XM_024446155.1:c.5197_5202+6del
XM_024446156.1:c.5197_5202+6del
XM_024446158.1:c.5197_5202+6del
XM_024446159.1:c.4948_4953+6del
XM_024446162.1:c.1738_1743+6del
XM_024446163.1:c.1498_1503+6del
NM_022455.5:c.6004_6009+6del
NM_172349.3:c.5197_5202+6del