Canonical Allele Identifier: CA2695205716
Gene: NSD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177282586_177282589del , CM000667.2:g.177282586_177282589del GRCh38
NC_000005.9:g.176709587_176709590del , CM000667.1:g.176709587_176709590del GRCh37
NC_000005.8:g.176642193_176642196del NCBI36
NG_009821.1:g.154508_154511del , LRG_512:g.154508_154511del

Transcript Alleles

HGVS Amino-acid Change
ENST00000508896.7:c.5136+5_5136+8del
ENST00000347982.9:c.5136+5_5136+8del
ENST00000354179.9:c.5136+5_5136+8del
ENST00000503056.6:c.651+5_651+8del
ENST00000508029.6:c.651+5_651+8del
ENST00000685206.1:n.5592+5_5592+8del
ENST00000686993.1:c.5136+5_5136+8del
ENST00000687453.1:c.5700+5_5700+8del
ENST00000688613.1:n.5406+5_5406+8del
ENST00000689345.1:c.5136+5_5136+8del
ENST00000689549.1:n.6156+5_6156+8del
ENST00000692024.1:n.4558+5_4558+8del
ENST00000439151.7:c.6009+5_6009+8del
ENST00000347982.8:c.5202+5_5202+8del
ENST00000354179.8:c.5202+5_5202+8del
ENST00000439151.6:c.6009+5_6009+8del
NM_022455.4:c.6009+5_6009+8del , LRG_512t1:c.6009+5_6009+8del
NM_172349.2:c.5202+5_5202+8del
XM_005265959.1:c.6009+5_6009+8del
XM_005265960.1:c.5202+5_5202+8del
XM_005265961.1:c.5202+5_5202+8del
XM_005265962.3:c.1503+5_1503+8del
XM_011534610.1:c.6009+5_6009+8del
XM_011534611.1:c.6009+5_6009+8del
XM_011534612.1:c.5589+5_5589+8del
XM_011534613.1:c.4953+5_4953+8del
XM_011534617.1:c.1743+5_1743+8del
NM_001365684.1:c.5202+5_5202+8del
XM_024446150.1:c.6009+5_6009+8del
XM_024446151.1:c.6009+5_6009+8del
XM_024446152.1:c.6009+5_6009+8del
XM_024446153.1:c.6009+5_6009+8del
XM_024446154.1:c.5589+5_5589+8del
XM_024446155.1:c.5202+5_5202+8del
XM_024446156.1:c.5202+5_5202+8del
XM_024446158.1:c.5202+5_5202+8del
XM_024446159.1:c.4953+5_4953+8del
XM_024446162.1:c.1743+5_1743+8del
XM_024446163.1:c.1503+5_1503+8del
NM_022455.5:c.6009+5_6009+8del
NM_172349.3:c.5202+5_5202+8del