Canonical Allele Identifier: CA2769562743

Gene: NSD1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177292101_177292102insACCAAACACACCCAACA , CM000667.2:g.177292101_177292102insACCAAACACACCCAACA	GRCh38
NC_000005.9:g.176719102_176719103insACCAAACACACCCAACA , CM000667.1:g.176719102_176719103insACCAAACACACCCAACA	GRCh37
NC_000005.8:g.176651708_176651709insACCAAACACACCCAACA	NCBI36
NG_009821.1:g.164023_164024insACCAAACACACCCAACA , LRG_512:g.164023_164024insACCAAACACACCCAACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508896.7:c.5533_5534insACCAAACACACCCAACA	ENSP00000423372.3:p.Pro1845HisfsTer20
ENST00000347982.9:c.5533_5534insACCAAACACACCCAACA	ENSP00000343209.5:p.Pro1845HisfsTer20
ENST00000354179.9:c.5533_5534insACCAAACACACCCAACA	ENSP00000346111.5:p.Pro1845HisfsTer20
ENST00000503056.6:c.1048_1049insACCAAACACACCCAACA	ENSP00000424024.2:p.Pro350HisfsTer20
ENST00000508029.6:c.1048_1049insACCAAACACACCCAACA	ENSP00000425120.2:p.Pro350HisfsTer20
ENST00000685206.1:n.5989_5990insACCAAACACACCCAACA
ENST00000686385.1:n.822_823insACCAAACACACCCAACA
ENST00000686993.1:c.5533_5534insACCAAACACACCCAACA	ENSP00000510020.1:p.Pro1845HisfsTer20
ENST00000687453.1:c.6097_6098insACCAAACACACCCAACA	ENSP00000508426.1:p.Pro2033HisfsTer20
ENST00000688613.1:n.5803_5804insACCAAACACACCCAACA
ENST00000689345.1:c.5533_5534insACCAAACACACCCAACA	ENSP00000509711.1:p.Pro1845HisfsTer20
ENST00000439151.7:c.6406_6407insACCAAACACACCCAACA MANE Select	ENSP00000395929.2:p.Pro2136HisfsTer20
ENST00000347982.8:c.5599_5600insACCAAACACACCCAACA	ENSP00000343209.4:p.Pro1867HisfsTer20
ENST00000354179.8:c.5599_5600insACCAAACACACCCAACA	ENSP00000346111.4:p.Pro1867HisfsTer20
ENST00000439151.6:c.6406_6407insACCAAACACACCCAACA	ENSP00000395929.2:p.Pro2136HisfsTer20
ENST00000513736.1:n.548_549insACCAAACACACCCAACA
NM_022455.4:c.6406_6407insACCAAACACACCCAACA , LRG_512t1:c.6406_6407insACCAAACACACCCAACA	NP_071900.2:p.Pro2136HisfsTer20
NM_172349.2:c.5599_5600insACCAAACACACCCAACA	NP_758859.1:p.Pro1867HisfsTer20
XM_005265959.1:c.6406_6407insACCAAACACACCCAACA	XP_005266016.1:p.Pro2136HisfsTer20
XM_005265960.1:c.5599_5600insACCAAACACACCCAACA	XP_005266017.1:p.Pro1867HisfsTer20
XM_005265961.1:c.5599_5600insACCAAACACACCCAACA	XP_005266018.1:p.Pro1867HisfsTer20
XM_005265962.3:c.1900_1901insACCAAACACACCCAACA	XP_005266019.1:p.Pro634HisfsTer20
XM_011534610.1:c.6406_6407insACCAAACACACCCAACA	XP_011532912.1:p.Pro2136HisfsTer20
XM_011534611.1:c.6406_6407insACCAAACACACCCAACA	XP_011532913.1:p.Pro2136HisfsTer20
XM_011534612.1:c.5986_5987insACCAAACACACCCAACA	XP_011532914.1:p.Pro1996HisfsTer20
XM_011534613.1:c.5350_5351insACCAAACACACCCAACA	XP_011532915.1:p.Pro1784HisfsTer20
XM_011534617.1:c.2140_2141insACCAAACACACCCAACA	XP_011532919.1:p.Pro714HisfsTer20
NM_001365684.1:c.5599_5600insACCAAACACACCCAACA	NP_001352613.1:p.Pro1867HisfsTer20
XM_024446150.1:c.6406_6407insACCAAACACACCCAACA	XP_024301918.1:p.Pro2136HisfsTer20
XM_024446151.1:c.6406_6407insACCAAACACACCCAACA	XP_024301919.1:p.Pro2136HisfsTer20
XM_024446152.1:c.6406_6407insACCAAACACACCCAACA	XP_024301920.1:p.Pro2136HisfsTer20
XM_024446153.1:c.6406_6407insACCAAACACACCCAACA	XP_024301921.1:p.Pro2136HisfsTer20
XM_024446154.1:c.5986_5987insACCAAACACACCCAACA	XP_024301922.1:p.Pro1996HisfsTer20
XM_024446155.1:c.5599_5600insACCAAACACACCCAACA	XP_024301923.1:p.Pro1867HisfsTer20
XM_024446156.1:c.5599_5600insACCAAACACACCCAACA	XP_024301924.1:p.Pro1867HisfsTer20
XM_024446158.1:c.5599_5600insACCAAACACACCCAACA	XP_024301926.1:p.Pro1867HisfsTer20
XM_024446159.1:c.5350_5351insACCAAACACACCCAACA	XP_024301927.1:p.Pro1784HisfsTer20
XM_024446162.1:c.2140_2141insACCAAACACACCCAACA	XP_024301930.1:p.Pro714HisfsTer20
XM_024446163.1:c.1900_1901insACCAAACACACCCAACA	XP_024301931.1:p.Pro634HisfsTer20
NM_022455.5:c.6406_6407insACCAAACACACCCAACA MANE Select	NP_071900.2:p.Pro2136HisfsTer20
NM_172349.3:c.5599_5600insACCAAACACACCCAACA	NP_758859.1:p.Pro1867HisfsTer20