Canonical Allele Identifier: CA1603532724

Gene: NSD1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177292005_177292007delinsCAG , CM000667.2:g.177292005_177292007delinsCAG	GRCh38
NC_000005.9:g.176719006_176719008delinsCAG , CM000667.1:g.176719006_176719008delinsCAG	GRCh37
NC_000005.8:g.176651612_176651614delinsCAG	NCBI36
NG_009821.1:g.163927_163929delinsCAG , LRG_512:g.163927_163929delinsCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508896.7:c.5437_5439delinsCAG	ENSP00000423372.3:p.Gln1813=
ENST00000347982.9:c.5437_5439delinsCAG	ENSP00000343209.5:p.Gln1813=
ENST00000354179.9:c.5437_5439delinsCAG	ENSP00000346111.5:p.Gln1813=
ENST00000503056.6:c.952_954delinsCAG	ENSP00000424024.2:p.Gln318=
ENST00000508029.6:c.952_954delinsCAG	ENSP00000425120.2:p.Gln318=
ENST00000685206.1:n.5893_5895delinsCAG
ENST00000686385.1:n.726_728delinsCAG
ENST00000686993.1:c.5437_5439delinsCAG	ENSP00000510020.1:p.Gln1813=
ENST00000687453.1:c.6001_6003delinsCAG	ENSP00000508426.1:p.Gln2001=
ENST00000688613.1:n.5707_5709delinsCAG
ENST00000689345.1:c.5437_5439delinsCAG	ENSP00000509711.1:p.Gln1813=
ENST00000439151.7:c.6310_6312delinsCAG MANE Select	ENSP00000395929.2:p.Gln2104=
ENST00000347982.8:c.5503_5505delinsCAG	ENSP00000343209.4:p.Gln1835=
ENST00000354179.8:c.5503_5505delinsCAG	ENSP00000346111.4:p.Gln1835=
ENST00000439151.6:c.6310_6312delinsCAG	ENSP00000395929.2:p.Gln2104=
ENST00000513736.1:n.452_454delinsCAG
NM_022455.4:c.6310_6312delinsCAG , LRG_512t1:c.6310_6312delinsCAG	NP_071900.2:p.Gln2104=
NM_172349.2:c.5503_5505delinsCAG	NP_758859.1:p.Gln1835=
XM_005265959.1:c.6310_6312delinsCAG	XP_005266016.1:p.Gln2104=
XM_005265960.1:c.5503_5505delinsCAG	XP_005266017.1:p.Gln1835=
XM_005265961.1:c.5503_5505delinsCAG	XP_005266018.1:p.Gln1835=
XM_005265962.3:c.1804_1806delinsCAG	XP_005266019.1:p.Gln602=
XM_011534610.1:c.6310_6312delinsCAG	XP_011532912.1:p.Gln2104=
XM_011534611.1:c.6310_6312delinsCAG	XP_011532913.1:p.Gln2104=
XM_011534612.1:c.5890_5892delinsCAG	XP_011532914.1:p.Gln1964=
XM_011534613.1:c.5254_5256delinsCAG	XP_011532915.1:p.Gln1752=
XM_011534617.1:c.2044_2046delinsCAG	XP_011532919.1:p.Gln682=
NM_001365684.1:c.5503_5505delinsCAG	NP_001352613.1:p.Gln1835=
XM_024446150.1:c.6310_6312delinsCAG	XP_024301918.1:p.Gln2104=
XM_024446151.1:c.6310_6312delinsCAG	XP_024301919.1:p.Gln2104=
XM_024446152.1:c.6310_6312delinsCAG	XP_024301920.1:p.Gln2104=
XM_024446153.1:c.6310_6312delinsCAG	XP_024301921.1:p.Gln2104=
XM_024446154.1:c.5890_5892delinsCAG	XP_024301922.1:p.Gln1964=
XM_024446155.1:c.5503_5505delinsCAG	XP_024301923.1:p.Gln1835=
XM_024446156.1:c.5503_5505delinsCAG	XP_024301924.1:p.Gln1835=
XM_024446158.1:c.5503_5505delinsCAG	XP_024301926.1:p.Gln1835=
XM_024446159.1:c.5254_5256delinsCAG	XP_024301927.1:p.Gln1752=
XM_024446162.1:c.2044_2046delinsCAG	XP_024301930.1:p.Gln682=
XM_024446163.1:c.1804_1806delinsCAG	XP_024301931.1:p.Gln602=
NM_022455.5:c.6310_6312delinsCAG MANE Select	NP_071900.2:p.Gln2104=
NM_172349.3:c.5503_5505delinsCAG	NP_758859.1:p.Gln1835=