Canonical Allele Identifier: CA808059631

Gene: NSD1

Linked Data

• dbSNP Id: rs1417306070
• MyVariant Identifiers: chr5:g.176718911_176718913del (hg19) ; chr5:g.177291910_177291912del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177291911_177291913del , CM000667.2:g.177291911_177291913del	GRCh38
NC_000005.9:g.176718912_176718914del , CM000667.1:g.176718912_176718914del	GRCh37
NC_000005.8:g.176651518_176651520del	NCBI36
NG_009821.1:g.163833_163835del , LRG_512:g.163833_163835del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508896.7:c.5386-43_5386-41del	ENSP00000423372.3:n.5386-43_5386-41del
ENST00000347982.9:c.5386-43_5386-41del	ENSP00000343209.5:n.5386-43_5386-41del
ENST00000354179.9:c.5386-43_5386-41del	ENSP00000346111.5:n.5386-43_5386-41del
ENST00000503056.6:c.901-43_901-41del	ENSP00000424024.2:n.901-43_901-41del
ENST00000508029.6:c.901-43_901-41del	ENSP00000425120.2:n.901-43_901-41del
ENST00000685206.1:n.5842-43_5842-41del
ENST00000686385.1:n.632_634del
ENST00000686993.1:c.5386-43_5386-41del	ENSP00000510020.1:n.5386-43_5386-41del
ENST00000687453.1:c.5950-43_5950-41del	ENSP00000508426.1:n.5950-43_5950-41del
ENST00000688613.1:n.5656-43_5656-41del
ENST00000689345.1:c.5386-43_5386-41del	ENSP00000509711.1:n.5386-43_5386-41del
ENST00000439151.7:c.6259-43_6259-41del MANE Select	ENSP00000395929.2:n.6259-43_6259-41del
ENST00000347982.8:c.5452-43_5452-41del	ENSP00000343209.4:n.5452-43_5452-41del
ENST00000354179.8:c.5452-43_5452-41del	ENSP00000346111.4:n.5452-43_5452-41del
ENST00000439151.6:c.6259-43_6259-41del	ENSP00000395929.2:n.6259-43_6259-41del
ENST00000513736.1:n.401-43_401-41del
NM_022455.4:c.6259-43_6259-41del , LRG_512t1:c.6259-43_6259-41del	NP_071900.2:n.6259-43_6259-41del
NM_172349.2:c.5452-43_5452-41del	NP_758859.1:n.5452-43_5452-41del
XM_005265959.1:c.6259-43_6259-41del	XP_005266016.1:n.6259-43_6259-41del
XM_005265960.1:c.5452-43_5452-41del	XP_005266017.1:n.5452-43_5452-41del
XM_005265961.1:c.5452-43_5452-41del	XP_005266018.1:n.5452-43_5452-41del
XM_005265962.3:c.1753-43_1753-41del	XP_005266019.1:n.1753-43_1753-41del
XM_011534610.1:c.6259-43_6259-41del	XP_011532912.1:n.6259-43_6259-41del
XM_011534611.1:c.6259-43_6259-41del	XP_011532913.1:n.6259-43_6259-41del
XM_011534612.1:c.5839-43_5839-41del	XP_011532914.1:n.5839-43_5839-41del
XM_011534613.1:c.5203-43_5203-41del	XP_011532915.1:n.5203-43_5203-41del
XM_011534617.1:c.1993-43_1993-41del	XP_011532919.1:n.1993-43_1993-41del
NM_001365684.1:c.5452-43_5452-41del	NP_001352613.1:n.5452-43_5452-41del
XM_024446150.1:c.6259-43_6259-41del	XP_024301918.1:n.6259-43_6259-41del
XM_024446151.1:c.6259-43_6259-41del	XP_024301919.1:n.6259-43_6259-41del
XM_024446152.1:c.6259-43_6259-41del	XP_024301920.1:n.6259-43_6259-41del
XM_024446153.1:c.6259-43_6259-41del	XP_024301921.1:n.6259-43_6259-41del
XM_024446154.1:c.5839-43_5839-41del	XP_024301922.1:n.5839-43_5839-41del
XM_024446155.1:c.5452-43_5452-41del	XP_024301923.1:n.5452-43_5452-41del
XM_024446156.1:c.5452-43_5452-41del	XP_024301924.1:n.5452-43_5452-41del
XM_024446158.1:c.5452-43_5452-41del	XP_024301926.1:n.5452-43_5452-41del
XM_024446159.1:c.5203-43_5203-41del	XP_024301927.1:n.5203-43_5203-41del
XM_024446162.1:c.1993-43_1993-41del	XP_024301930.1:n.1993-43_1993-41del
XM_024446163.1:c.1753-43_1753-41del	XP_024301931.1:n.1753-43_1753-41del
NM_022455.5:c.6259-43_6259-41del MANE Select	NP_071900.2:n.6259-43_6259-41del
NM_172349.3:c.5452-43_5452-41del	NP_758859.1:n.5452-43_5452-41del