Canonical Allele Identifier: CA294972
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 159373
ClinVar RCV Id: RCV003231273
dbSNP Id: rs587784152

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177273780_177273781del , CM000667.2:g.177273780_177273781del GRCh38
NC_000005.9:g.176700781_176700782del , CM000667.1:g.176700781_176700782del GRCh37
NC_000005.8:g.176633387_176633388del NCBI36
NG_009821.1:g.145702_145703del , LRG_512:g.145702_145703del

Transcript Alleles

HGVS Amino-acid change
ENST00000508896.7:c.4745_4746del ENSP00000423372.3:p.Ile1582LysfsTer18
ENST00000347982.9:c.4745_4746del ENSP00000343209.5:p.Ile1582LysfsTer18
ENST00000354179.9:c.4745_4746del ENSP00000346111.5:p.Ile1582LysfsTer18
ENST00000503056.6:c.260_261del ENSP00000424024.2:p.Ile87LysfsTer18
ENST00000508029.6:c.260_261del ENSP00000425120.2:p.Ile87LysfsTer18
ENST00000685206.1:n.5201_5202del
ENST00000686993.1:c.4745_4746del ENSP00000510020.1:p.Ile1582LysfsTer18
ENST00000687095.1:n.367_368del
ENST00000687453.1:c.5309_5310del ENSP00000508426.1:p.Ile1770LysfsTer18
ENST00000688613.1:n.5015_5016del
ENST00000689345.1:c.4745_4746del ENSP00000509711.1:p.Ile1582LysfsTer18
ENST00000689549.1:n.5765_5766del
ENST00000692024.1:n.2537_2538del
ENST00000439151.7:c.5618_5619del MANE Select ENSP00000395929.2:p.Ile1873LysfsTer18
ENST00000347982.8:c.4811_4812del ENSP00000343209.4:p.Ile1604LysfsTer18
ENST00000354179.8:c.4811_4812del ENSP00000346111.4:p.Ile1604LysfsTer18
ENST00000439151.6:c.5618_5619del ENSP00000395929.2:p.Ile1873LysfsTer18
ENST00000503056.5:c.260_261del ENSP00000424024.1:p.Ile87LysfsTer?
NM_022455.4:c.5618_5619del , LRG_512t1:c.5618_5619del NP_071900.2:p.Ile1873LysfsTer18
NM_172349.2:c.4811_4812del NP_758859.1:p.Ile1604LysfsTer18
XM_005265959.1:c.5618_5619del XP_005266016.1:p.Ile1873LysfsTer18
XM_005265960.1:c.4811_4812del XP_005266017.1:p.Ile1604LysfsTer18
XM_005265961.1:c.4811_4812del XP_005266018.1:p.Ile1604LysfsTer18
XM_005265962.3:c.1112_1113del XP_005266019.1:p.Ile371LysfsTer18
XM_011534610.1:c.5618_5619del XP_011532912.1:p.Ile1873LysfsTer18
XM_011534611.1:c.5618_5619del XP_011532913.1:p.Ile1873LysfsTer18
XM_011534612.1:c.5198_5199del XP_011532914.1:p.Ile1733LysfsTer18
XM_011534613.1:c.4562_4563del XP_011532915.1:p.Ile1521LysfsTer18
XM_011534617.1:c.1352_1353del XP_011532919.1:p.Ile451LysfsTer18
NM_001365684.1:c.4811_4812del NP_001352613.1:p.Ile1604LysfsTer18
XM_024446150.1:c.5618_5619del XP_024301918.1:p.Ile1873LysfsTer18
XM_024446151.1:c.5618_5619del XP_024301919.1:p.Ile1873LysfsTer18
XM_024446152.1:c.5618_5619del XP_024301920.1:p.Ile1873LysfsTer18
XM_024446153.1:c.5618_5619del XP_024301921.1:p.Ile1873LysfsTer18
XM_024446154.1:c.5198_5199del XP_024301922.1:p.Ile1733LysfsTer18
XM_024446155.1:c.4811_4812del XP_024301923.1:p.Ile1604LysfsTer18
XM_024446156.1:c.4811_4812del XP_024301924.1:p.Ile1604LysfsTer18
XM_024446158.1:c.4811_4812del XP_024301926.1:p.Ile1604LysfsTer18
XM_024446159.1:c.4562_4563del XP_024301927.1:p.Ile1521LysfsTer18
XM_024446162.1:c.1352_1353del XP_024301930.1:p.Ile451LysfsTer18
XM_024446163.1:c.1112_1113del XP_024301931.1:p.Ile371LysfsTer18
NM_022455.5:c.5618_5619del MANE Select NP_071900.2:p.Ile1873LysfsTer18
NM_172349.3:c.4811_4812del NP_758859.1:p.Ile1604LysfsTer18