Canonical Allele Identifier: CA1603552196

Gene: NSD1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177282625_177282626delinsAT , CM000667.2:g.177282625_177282626delinsAT	GRCh38
NC_000005.9:g.176709626_176709627delinsAT , CM000667.1:g.176709626_176709627delinsAT	GRCh37
NC_000005.8:g.176642232_176642233delinsAT	NCBI36
NG_009821.1:g.154547_154548delinsAT , LRG_512:g.154547_154548delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508896.7:c.5136+44_5136+45delinsAT	ENSP00000423372.3:n.5136+44_5136+45delinsAT
ENST00000347982.9:c.5136+44_5136+45delinsAT	ENSP00000343209.5:n.5136+44_5136+45delinsAT
ENST00000354179.9:c.5136+44_5136+45delinsAT	ENSP00000346111.5:n.5136+44_5136+45delinsAT
ENST00000503056.6:c.651+44_651+45delinsAT	ENSP00000424024.2:n.651+44_651+45delinsAT
ENST00000508029.6:c.651+44_651+45delinsAT	ENSP00000425120.2:n.651+44_651+45delinsAT
ENST00000685206.1:n.5592+44_5592+45delinsAT
ENST00000686993.1:c.5136+44_5136+45delinsAT	ENSP00000510020.1:n.5136+44_5136+45delinsAT
ENST00000687453.1:c.5700+44_5700+45delinsAT	ENSP00000508426.1:n.5700+44_5700+45delinsAT
ENST00000688613.1:n.5406+44_5406+45delinsAT
ENST00000689345.1:c.5136+44_5136+45delinsAT	ENSP00000509711.1:n.5136+44_5136+45delinsAT
ENST00000689549.1:n.6156+44_6156+45delinsAT
ENST00000692024.1:n.4558+44_4558+45delinsAT
ENST00000439151.7:c.6009+44_6009+45delinsAT MANE Select	ENSP00000395929.2:n.6009+44_6009+45delinsAT
ENST00000347982.8:c.5202+44_5202+45delinsAT	ENSP00000343209.4:n.5202+44_5202+45delinsAT
ENST00000354179.8:c.5202+44_5202+45delinsAT	ENSP00000346111.4:n.5202+44_5202+45delinsAT
ENST00000439151.6:c.6009+44_6009+45delinsAT	ENSP00000395929.2:n.6009+44_6009+45delinsAT
NM_022455.4:c.6009+44_6009+45delinsAT , LRG_512t1:c.6009+44_6009+45delinsAT	NP_071900.2:n.6009+44_6009+45delinsAT
NM_172349.2:c.5202+44_5202+45delinsAT	NP_758859.1:n.5202+44_5202+45delinsAT
XM_005265959.1:c.6009+44_6009+45delinsAT	XP_005266016.1:n.6009+44_6009+45delinsAT
XM_005265960.1:c.5202+44_5202+45delinsAT	XP_005266017.1:n.5202+44_5202+45delinsAT
XM_005265961.1:c.5202+44_5202+45delinsAT	XP_005266018.1:n.5202+44_5202+45delinsAT
XM_005265962.3:c.1503+44_1503+45delinsAT	XP_005266019.1:n.1503+44_1503+45delinsAT
XM_011534610.1:c.6009+44_6009+45delinsAT	XP_011532912.1:n.6009+44_6009+45delinsAT
XM_011534611.1:c.6009+44_6009+45delinsAT	XP_011532913.1:n.6009+44_6009+45delinsAT
XM_011534612.1:c.5589+44_5589+45delinsAT	XP_011532914.1:n.5589+44_5589+45delinsAT
XM_011534613.1:c.4953+44_4953+45delinsAT	XP_011532915.1:n.4953+44_4953+45delinsAT
XM_011534617.1:c.1743+44_1743+45delinsAT	XP_011532919.1:n.1743+44_1743+45delinsAT
NM_001365684.1:c.5202+44_5202+45delinsAT	NP_001352613.1:n.5202+44_5202+45delinsAT
XM_024446150.1:c.6009+44_6009+45delinsAT	XP_024301918.1:n.6009+44_6009+45delinsAT
XM_024446151.1:c.6009+44_6009+45delinsAT	XP_024301919.1:n.6009+44_6009+45delinsAT
XM_024446152.1:c.6009+44_6009+45delinsAT	XP_024301920.1:n.6009+44_6009+45delinsAT
XM_024446153.1:c.6009+44_6009+45delinsAT	XP_024301921.1:n.6009+44_6009+45delinsAT
XM_024446154.1:c.5589+44_5589+45delinsAT	XP_024301922.1:n.5589+44_5589+45delinsAT
XM_024446155.1:c.5202+44_5202+45delinsAT	XP_024301923.1:n.5202+44_5202+45delinsAT
XM_024446156.1:c.5202+44_5202+45delinsAT	XP_024301924.1:n.5202+44_5202+45delinsAT
XM_024446158.1:c.5202+44_5202+45delinsAT	XP_024301926.1:n.5202+44_5202+45delinsAT
XM_024446159.1:c.4953+44_4953+45delinsAT	XP_024301927.1:n.4953+44_4953+45delinsAT
XM_024446162.1:c.1743+44_1743+45delinsAT	XP_024301930.1:n.1743+44_1743+45delinsAT
XM_024446163.1:c.1503+44_1503+45delinsAT	XP_024301931.1:n.1503+44_1503+45delinsAT
NM_022455.5:c.6009+44_6009+45delinsAT MANE Select	NP_071900.2:n.6009+44_6009+45delinsAT
NM_172349.3:c.5202+44_5202+45delinsAT	NP_758859.1:n.5202+44_5202+45delinsAT