Canonical Allele Identifier: CA2695205715

Gene: NSD1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177282576_177282579del , CM000667.2:g.177282576_177282579del	GRCh38
NC_000005.9:g.176709577_176709580del , CM000667.1:g.176709577_176709580del	GRCh37
NC_000005.8:g.176642183_176642186del	NCBI36
NG_009821.1:g.154498_154501del , LRG_512:g.154498_154501del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508896.7:c.5131_5134del	ENSP00000423372.3:p.Asp1711LysfsTer17
ENST00000347982.9:c.5131_5134del	ENSP00000343209.5:p.Asp1711LysfsTer17
ENST00000354179.9:c.5131_5134del	ENSP00000346111.5:p.Asp1711LysfsTer17
ENST00000503056.6:c.646_649del	ENSP00000424024.2:p.Asp216LysfsTer17
ENST00000508029.6:c.646_649del	ENSP00000425120.2:p.Asp216LysfsTer17
ENST00000685206.1:n.5587_5590del
ENST00000686993.1:c.5131_5134del	ENSP00000510020.1:p.Asp1711LysfsTer17
ENST00000687453.1:c.5695_5698del	ENSP00000508426.1:p.Asp1899LysfsTer17
ENST00000688613.1:n.5401_5404del
ENST00000689345.1:c.5131_5134del	ENSP00000509711.1:p.Asp1711LysfsTer17
ENST00000689549.1:n.6151_6154del
ENST00000692024.1:n.4553_4556del
ENST00000439151.7:c.6004_6007del MANE Select	ENSP00000395929.2:p.Asp2002LysfsTer17
ENST00000347982.8:c.5197_5200del	ENSP00000343209.4:p.Asp1733LysfsTer17
ENST00000354179.8:c.5197_5200del	ENSP00000346111.4:p.Asp1733LysfsTer17
ENST00000439151.6:c.6004_6007del	ENSP00000395929.2:p.Asp2002LysfsTer17
NM_022455.4:c.6004_6007del , LRG_512t1:c.6004_6007del	NP_071900.2:p.Asp2002LysfsTer17
NM_172349.2:c.5197_5200del	NP_758859.1:p.Asp1733LysfsTer17
XM_005265959.1:c.6004_6007del	XP_005266016.1:p.Asp2002LysfsTer17
XM_005265960.1:c.5197_5200del	XP_005266017.1:p.Asp1733LysfsTer17
XM_005265961.1:c.5197_5200del	XP_005266018.1:p.Asp1733LysfsTer17
XM_005265962.3:c.1498_1501del	XP_005266019.1:p.Asp500LysfsTer17
XM_011534610.1:c.6004_6007del	XP_011532912.1:p.Asp2002LysfsTer17
XM_011534611.1:c.6004_6007del	XP_011532913.1:p.Asp2002LysfsTer17
XM_011534612.1:c.5584_5587del	XP_011532914.1:p.Asp1862LysfsTer17
XM_011534613.1:c.4948_4951del	XP_011532915.1:p.Asp1650LysfsTer17
XM_011534617.1:c.1738_1741del	XP_011532919.1:p.Asp580LysfsTer17
NM_001365684.1:c.5197_5200del	NP_001352613.1:p.Asp1733LysfsTer17
XM_024446150.1:c.6004_6007del	XP_024301918.1:p.Asp2002LysfsTer17
XM_024446151.1:c.6004_6007del	XP_024301919.1:p.Asp2002LysfsTer17
XM_024446152.1:c.6004_6007del	XP_024301920.1:p.Asp2002LysfsTer17
XM_024446153.1:c.6004_6007del	XP_024301921.1:p.Asp2002LysfsTer17
XM_024446154.1:c.5584_5587del	XP_024301922.1:p.Asp1862LysfsTer17
XM_024446155.1:c.5197_5200del	XP_024301923.1:p.Asp1733LysfsTer17
XM_024446156.1:c.5197_5200del	XP_024301924.1:p.Asp1733LysfsTer17
XM_024446158.1:c.5197_5200del	XP_024301926.1:p.Asp1733LysfsTer17
XM_024446159.1:c.4948_4951del	XP_024301927.1:p.Asp1650LysfsTer17
XM_024446162.1:c.1738_1741del	XP_024301930.1:p.Asp580LysfsTer17
XM_024446163.1:c.1498_1501del	XP_024301931.1:p.Asp500LysfsTer17
NM_022455.5:c.6004_6007del MANE Select	NP_071900.2:p.Asp2002LysfsTer17
NM_172349.3:c.5197_5200del	NP_758859.1:p.Asp1733LysfsTer17