Canonical Allele Identifier: CA2711007703

Gene: NSD1

Linked Data

• dbSNP Id: rs2127261058

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177282580_177282581insGAAATACCTCCTG , CM000667.2:g.177282580_177282581insGAAATACCTCCTG	GRCh38
NC_000005.9:g.176709581_176709582insGAAATACCTCCTG , CM000667.1:g.176709581_176709582insGAAATACCTCCTG	GRCh37
NC_000005.8:g.176642187_176642188insGAAATACCTCCTG	NCBI36
NG_009821.1:g.154502_154503insGAAATACCTCCTG , LRG_512:g.154502_154503insGAAATACCTCCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508896.7:c.5135_5136insGAAATACCTCCTG	ENSP00000423372.3:p.Asp1713LysfsTer9
ENST00000347982.9:c.5135_5136insGAAATACCTCCTG	ENSP00000343209.5:p.Asp1713LysfsTer9
ENST00000354179.9:c.5135_5136insGAAATACCTCCTG	ENSP00000346111.5:p.Asp1713LysfsTer9
ENST00000503056.6:c.650_651insGAAATACCTCCTG	ENSP00000424024.2:p.Asp218LysfsTer9
ENST00000508029.6:c.650_651insGAAATACCTCCTG	ENSP00000425120.2:p.Asp218LysfsTer9
ENST00000685206.1:n.5591_5592insGAAATACCTCCTG
ENST00000686993.1:c.5135_5136insGAAATACCTCCTG	ENSP00000510020.1:p.Asp1713LysfsTer9
ENST00000687453.1:c.5699_5700insGAAATACCTCCTG	ENSP00000508426.1:p.Asp1901LysfsTer9
ENST00000688613.1:n.5405_5406insGAAATACCTCCTG
ENST00000689345.1:c.5135_5136insGAAATACCTCCTG	ENSP00000509711.1:p.Asp1713LysfsTer9
ENST00000689549.1:n.6155_6156insGAAATACCTCCTG
ENST00000692024.1:n.4557_4558insGAAATACCTCCTG
ENST00000439151.7:c.6008_6009insGAAATACCTCCTG MANE Select	ENSP00000395929.2:p.Asp2004LysfsTer9
ENST00000347982.8:c.5201_5202insGAAATACCTCCTG	ENSP00000343209.4:p.Asp1735LysfsTer9
ENST00000354179.8:c.5201_5202insGAAATACCTCCTG	ENSP00000346111.4:p.Asp1735LysfsTer9
ENST00000439151.6:c.6008_6009insGAAATACCTCCTG	ENSP00000395929.2:p.Asp2004LysfsTer9
NM_022455.4:c.6008_6009insGAAATACCTCCTG , LRG_512t1:c.6008_6009insGAAATACCTCCTG	NP_071900.2:p.Asp2004LysfsTer9
NM_172349.2:c.5201_5202insGAAATACCTCCTG	NP_758859.1:p.Asp1735LysfsTer9
XM_005265959.1:c.6008_6009insGAAATACCTCCTG	XP_005266016.1:p.Asp2004LysfsTer9
XM_005265960.1:c.5201_5202insGAAATACCTCCTG	XP_005266017.1:p.Asp1735LysfsTer9
XM_005265961.1:c.5201_5202insGAAATACCTCCTG	XP_005266018.1:p.Asp1735LysfsTer9
XM_005265962.3:c.1502_1503insGAAATACCTCCTG	XP_005266019.1:p.Asp502LysfsTer9
XM_011534610.1:c.6008_6009insGAAATACCTCCTG	XP_011532912.1:p.Asp2004LysfsTer9
XM_011534611.1:c.6008_6009insGAAATACCTCCTG	XP_011532913.1:p.Asp2004LysfsTer9
XM_011534612.1:c.5588_5589insGAAATACCTCCTG	XP_011532914.1:p.Asp1864LysfsTer9
XM_011534613.1:c.4952_4953insGAAATACCTCCTG	XP_011532915.1:p.Asp1652LysfsTer9
XM_011534617.1:c.1742_1743insGAAATACCTCCTG	XP_011532919.1:p.Asp582LysfsTer9
NM_001365684.1:c.5201_5202insGAAATACCTCCTG	NP_001352613.1:p.Asp1735LysfsTer9
XM_024446150.1:c.6008_6009insGAAATACCTCCTG	XP_024301918.1:p.Asp2004LysfsTer9
XM_024446151.1:c.6008_6009insGAAATACCTCCTG	XP_024301919.1:p.Asp2004LysfsTer9
XM_024446152.1:c.6008_6009insGAAATACCTCCTG	XP_024301920.1:p.Asp2004LysfsTer9
XM_024446153.1:c.6008_6009insGAAATACCTCCTG	XP_024301921.1:p.Asp2004LysfsTer9
XM_024446154.1:c.5588_5589insGAAATACCTCCTG	XP_024301922.1:p.Asp1864LysfsTer9
XM_024446155.1:c.5201_5202insGAAATACCTCCTG	XP_024301923.1:p.Asp1735LysfsTer9
XM_024446156.1:c.5201_5202insGAAATACCTCCTG	XP_024301924.1:p.Asp1735LysfsTer9
XM_024446158.1:c.5201_5202insGAAATACCTCCTG	XP_024301926.1:p.Asp1735LysfsTer9
XM_024446159.1:c.4952_4953insGAAATACCTCCTG	XP_024301927.1:p.Asp1652LysfsTer9
XM_024446162.1:c.1742_1743insGAAATACCTCCTG	XP_024301930.1:p.Asp582LysfsTer9
XM_024446163.1:c.1502_1503insGAAATACCTCCTG	XP_024301931.1:p.Asp502LysfsTer9
NM_022455.5:c.6008_6009insGAAATACCTCCTG MANE Select	NP_071900.2:p.Asp2004LysfsTer9
NM_172349.3:c.5201_5202insGAAATACCTCCTG	NP_758859.1:p.Asp1735LysfsTer9