Canonical Allele Identifier: CA1603532513

Gene: NSD1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177291909_177291912delinsCTAA , CM000667.2:g.177291909_177291912delinsCTAA	GRCh38
NC_000005.9:g.176718910_176718913delinsCTAA , CM000667.1:g.176718910_176718913delinsCTAA	GRCh37
NC_000005.8:g.176651516_176651519delinsCTAA	NCBI36
NG_009821.1:g.163831_163834delinsCTAA , LRG_512:g.163831_163834delinsCTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508896.7:c.5386-45_5386-42delinsCTAA	ENSP00000423372.3:n.5386-45_5386-42delinsCTAA
ENST00000347982.9:c.5386-45_5386-42delinsCTAA	ENSP00000343209.5:n.5386-45_5386-42delinsCTAA
ENST00000354179.9:c.5386-45_5386-42delinsCTAA	ENSP00000346111.5:n.5386-45_5386-42delinsCTAA
ENST00000503056.6:c.901-45_901-42delinsCTAA	ENSP00000424024.2:n.901-45_901-42delinsCTAA
ENST00000508029.6:c.901-45_901-42delinsCTAA	ENSP00000425120.2:n.901-45_901-42delinsCTAA
ENST00000685206.1:n.5842-45_5842-42delinsCTAA
ENST00000686385.1:n.630_633delinsCTAA
ENST00000686993.1:c.5386-45_5386-42delinsCTAA	ENSP00000510020.1:n.5386-45_5386-42delinsCTAA
ENST00000687453.1:c.5950-45_5950-42delinsCTAA	ENSP00000508426.1:n.5950-45_5950-42delinsCTAA
ENST00000688613.1:n.5656-45_5656-42delinsCTAA
ENST00000689345.1:c.5386-45_5386-42delinsCTAA	ENSP00000509711.1:n.5386-45_5386-42delinsCTAA
ENST00000439151.7:c.6259-45_6259-42delinsCTAA MANE Select	ENSP00000395929.2:n.6259-45_6259-42delinsCTAA
ENST00000347982.8:c.5452-45_5452-42delinsCTAA	ENSP00000343209.4:n.5452-45_5452-42delinsCTAA
ENST00000354179.8:c.5452-45_5452-42delinsCTAA	ENSP00000346111.4:n.5452-45_5452-42delinsCTAA
ENST00000439151.6:c.6259-45_6259-42delinsCTAA	ENSP00000395929.2:n.6259-45_6259-42delinsCTAA
ENST00000513736.1:n.401-45_401-42delinsCTAA
NM_022455.4:c.6259-45_6259-42delinsCTAA , LRG_512t1:c.6259-45_6259-42delinsCTAA	NP_071900.2:n.6259-45_6259-42delinsCTAA
NM_172349.2:c.5452-45_5452-42delinsCTAA	NP_758859.1:n.5452-45_5452-42delinsCTAA
XM_005265959.1:c.6259-45_6259-42delinsCTAA	XP_005266016.1:n.6259-45_6259-42delinsCTAA
XM_005265960.1:c.5452-45_5452-42delinsCTAA	XP_005266017.1:n.5452-45_5452-42delinsCTAA
XM_005265961.1:c.5452-45_5452-42delinsCTAA	XP_005266018.1:n.5452-45_5452-42delinsCTAA
XM_005265962.3:c.1753-45_1753-42delinsCTAA	XP_005266019.1:n.1753-45_1753-42delinsCTAA
XM_011534610.1:c.6259-45_6259-42delinsCTAA	XP_011532912.1:n.6259-45_6259-42delinsCTAA
XM_011534611.1:c.6259-45_6259-42delinsCTAA	XP_011532913.1:n.6259-45_6259-42delinsCTAA
XM_011534612.1:c.5839-45_5839-42delinsCTAA	XP_011532914.1:n.5839-45_5839-42delinsCTAA
XM_011534613.1:c.5203-45_5203-42delinsCTAA	XP_011532915.1:n.5203-45_5203-42delinsCTAA
XM_011534617.1:c.1993-45_1993-42delinsCTAA	XP_011532919.1:n.1993-45_1993-42delinsCTAA
NM_001365684.1:c.5452-45_5452-42delinsCTAA	NP_001352613.1:n.5452-45_5452-42delinsCTAA
XM_024446150.1:c.6259-45_6259-42delinsCTAA	XP_024301918.1:n.6259-45_6259-42delinsCTAA
XM_024446151.1:c.6259-45_6259-42delinsCTAA	XP_024301919.1:n.6259-45_6259-42delinsCTAA
XM_024446152.1:c.6259-45_6259-42delinsCTAA	XP_024301920.1:n.6259-45_6259-42delinsCTAA
XM_024446153.1:c.6259-45_6259-42delinsCTAA	XP_024301921.1:n.6259-45_6259-42delinsCTAA
XM_024446154.1:c.5839-45_5839-42delinsCTAA	XP_024301922.1:n.5839-45_5839-42delinsCTAA
XM_024446155.1:c.5452-45_5452-42delinsCTAA	XP_024301923.1:n.5452-45_5452-42delinsCTAA
XM_024446156.1:c.5452-45_5452-42delinsCTAA	XP_024301924.1:n.5452-45_5452-42delinsCTAA
XM_024446158.1:c.5452-45_5452-42delinsCTAA	XP_024301926.1:n.5452-45_5452-42delinsCTAA
XM_024446159.1:c.5203-45_5203-42delinsCTAA	XP_024301927.1:n.5203-45_5203-42delinsCTAA
XM_024446162.1:c.1993-45_1993-42delinsCTAA	XP_024301930.1:n.1993-45_1993-42delinsCTAA
XM_024446163.1:c.1753-45_1753-42delinsCTAA	XP_024301931.1:n.1753-45_1753-42delinsCTAA
NM_022455.5:c.6259-45_6259-42delinsCTAA MANE Select	NP_071900.2:n.6259-45_6259-42delinsCTAA
NM_172349.3:c.5452-45_5452-42delinsCTAA	NP_758859.1:n.5452-45_5452-42delinsCTAA