Canonical Allele Identifier: CA1603533191

Gene: NSD1

Linked Data

• dbSNP Id: rs1757222009

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177264072_177264084dup , CM000667.2:g.177264072_177264084dup	GRCh38
NC_000005.9:g.176691073_176691085dup , CM000667.1:g.176691073_176691085dup	GRCh37
NC_000005.8:g.176623679_176623691dup	NCBI36
NG_009821.1:g.135994_136006dup , LRG_512:g.135994_136006dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000508896.7:c.4274-3490_4274-3478dup	ENSP00000423372.3:n.4274-3490_4274-3478dup
ENST00000347982.9:c.4274-3490_4274-3478dup	ENSP00000343209.5:n.4274-3490_4274-3478dup
ENST00000354179.9:c.4274-3490_4274-3478dup	ENSP00000346111.5:n.4274-3490_4274-3478dup
ENST00000685206.1:n.4730-3490_4730-3478dup
ENST00000686993.1:c.4274-3490_4274-3478dup	ENSP00000510020.1:n.4274-3490_4274-3478dup
ENST00000687453.1:c.4838-3490_4838-3478dup	ENSP00000508426.1:n.4838-3490_4838-3478dup
ENST00000688613.1:n.4544-3490_4544-3478dup
ENST00000689345.1:c.4274-3490_4274-3478dup	ENSP00000509711.1:n.4274-3490_4274-3478dup
ENST00000689549.1:n.5294-3490_5294-3478dup
ENST00000439151.7:c.5147-3490_5147-3478dup MANE Select	ENSP00000395929.2:n.5147-3490_5147-3478dup
ENST00000347982.8:c.4340-3490_4340-3478dup	ENSP00000343209.4:n.4340-3490_4340-3478dup
ENST00000354179.8:c.4340-3490_4340-3478dup	ENSP00000346111.4:n.4340-3490_4340-3478dup
ENST00000439151.6:c.5147-3490_5147-3478dup	ENSP00000395929.2:n.5147-3490_5147-3478dup
NM_022455.4:c.5147-3490_5147-3478dup , LRG_512t1:c.5147-3490_5147-3478dup	NP_071900.2:n.5147-3490_5147-3478dup
NM_172349.2:c.4340-3490_4340-3478dup	NP_758859.1:n.4340-3490_4340-3478dup
XM_005265959.1:c.5147-3490_5147-3478dup	XP_005266016.1:n.5147-3490_5147-3478dup
XM_005265960.1:c.4340-3490_4340-3478dup	XP_005266017.1:n.4340-3490_4340-3478dup
XM_005265961.1:c.4340-3490_4340-3478dup	XP_005266018.1:n.4340-3490_4340-3478dup
XM_005265962.3:c.641-3490_641-3478dup	XP_005266019.1:n.641-3490_641-3478dup
XM_011534610.1:c.5147-3490_5147-3478dup	XP_011532912.1:n.5147-3490_5147-3478dup
XM_011534611.1:c.5147-3490_5147-3478dup	XP_011532913.1:n.5147-3490_5147-3478dup
XM_011534612.1:c.4727-3490_4727-3478dup	XP_011532914.1:n.4727-3490_4727-3478dup
XM_011534613.1:c.4091-3490_4091-3478dup	XP_011532915.1:n.4091-3490_4091-3478dup
XM_011534617.1:c.881-3490_881-3478dup	XP_011532919.1:n.881-3490_881-3478dup
NM_001365684.1:c.4340-3490_4340-3478dup	NP_001352613.1:n.4340-3490_4340-3478dup
XM_024446150.1:c.5147-3490_5147-3478dup	XP_024301918.1:n.5147-3490_5147-3478dup
XM_024446151.1:c.5147-3490_5147-3478dup	XP_024301919.1:n.5147-3490_5147-3478dup
XM_024446152.1:c.5147-3490_5147-3478dup	XP_024301920.1:n.5147-3490_5147-3478dup
XM_024446153.1:c.5147-3490_5147-3478dup	XP_024301921.1:n.5147-3490_5147-3478dup
XM_024446154.1:c.4727-3490_4727-3478dup	XP_024301922.1:n.4727-3490_4727-3478dup
XM_024446155.1:c.4340-3490_4340-3478dup	XP_024301923.1:n.4340-3490_4340-3478dup
XM_024446156.1:c.4340-3490_4340-3478dup	XP_024301924.1:n.4340-3490_4340-3478dup
XM_024446158.1:c.4340-3490_4340-3478dup	XP_024301926.1:n.4340-3490_4340-3478dup
XM_024446159.1:c.4091-3490_4091-3478dup	XP_024301927.1:n.4091-3490_4091-3478dup
XM_024446162.1:c.881-3490_881-3478dup	XP_024301930.1:n.881-3490_881-3478dup
XM_024446163.1:c.641-3490_641-3478dup	XP_024301931.1:n.641-3490_641-3478dup
NM_022455.5:c.5147-3490_5147-3478dup MANE Select	NP_071900.2:n.5147-3490_5147-3478dup
NM_172349.3:c.4340-3490_4340-3478dup	NP_758859.1:n.4340-3490_4340-3478dup