Canonical Allele Identifier: CA294782
Gene: NSD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177204133del , CM000667.2:g.177204133del GRCh38
NC_000005.9:g.176631134del , CM000667.1:g.176631134del GRCh37
NC_000005.8:g.176563740del NCBI36
NG_009821.1:g.76055del , LRG_512:g.76055del

Transcript Alleles

HGVS Amino-acid Change
ENST00000508896.7:c.204del ENSP00000423372.3:p.Arg68SerfsTer?
ENST00000347982.9:c.204del ENSP00000343209.5:p.Arg68SerfsTer?
ENST00000354179.9:c.204del ENSP00000346111.5:p.Arg68SerfsTer?
ENST00000508896.6:c.204del ENSP00000423372.2:p.Arg68SerfsTer?
ENST00000510954.6:n.453del
ENST00000638627.3:c.21del ENSP00000492679.3:p.Arg7SerfsTer?
ENST00000644863.2:c.21del ENSP00000496157.2:p.Arg7SerfsTer?
ENST00000685206.1:n.660del
ENST00000686993.1:c.204del ENSP00000510020.1:p.Arg68SerfsTer?
ENST00000687453.1:c.928-5503del ENSP00000508426.1:n.928-5503del
ENST00000688613.1:n.474del
ENST00000689326.1:c.1077del ENSP00000509594.1:p.Arg359SerfsTer?
ENST00000689345.1:c.204del ENSP00000509711.1:p.Arg68SerfsTer?
ENST00000689549.1:n.1224del
ENST00000439151.7:c.1077del MANE Select ENSP00000395929.2:p.Arg359SerfsTer?
ENST00000638627.2:c.*170del ENSP00000492679.2:n.*170del
ENST00000644863.1:c.*386del ENSP00000496157.1:n.*386del
ENST00000347982.8:c.270del ENSP00000343209.4:p.Arg90SerfsTer?
ENST00000354179.8:c.270del ENSP00000346111.4:p.Arg90SerfsTer?
ENST00000439151.6:c.1077del ENSP00000395929.2:p.Arg359SerfsTer?
ENST00000508896.5:c.270del ENSP00000423372.1:p.Arg90SerfsTer?
ENST00000510954.5:c.270del ENSP00000423982.1:p.Arg90SerfsTer?
NM_022455.4:c.1077del , LRG_512t1:c.1077del NP_071900.2:p.Arg359SerfsTer?
NM_172349.2:c.270del NP_758859.1:p.Arg90SerfsTer?
XM_005265959.1:c.1077del XP_005266016.1:p.Arg359SerfsTer?
XM_005265960.1:c.270del XP_005266017.1:p.Arg90SerfsTer?
XM_005265961.1:c.270del XP_005266018.1:p.Arg90SerfsTer?
XM_011534610.1:c.1077del XP_011532912.1:p.Arg359SerfsTer?
XM_011534611.1:c.1077del XP_011532913.1:p.Arg359SerfsTer?
XM_011534612.1:c.657del XP_011532914.1:p.Arg219SerfsTer?
XM_011534613.1:c.21del XP_011532915.1:p.Arg7SerfsTer?
XM_011534614.1:c.1077del XP_011532916.1:p.Arg359SerfsTer?
XM_011534615.1:c.1077del XP_011532917.1:p.Arg359SerfsTer?
XM_011534616.1:c.1077del XP_011532918.1:p.Arg359SerfsTer?
NM_001365684.1:c.270del NP_001352613.1:p.Arg90SerfsTer?
XM_024446150.1:c.1077del XP_024301918.1:p.Arg359SerfsTer?
XM_024446151.1:c.1077del XP_024301919.1:p.Arg359SerfsTer?
XM_024446152.1:c.1077del XP_024301920.1:p.Arg359SerfsTer?
XM_024446153.1:c.1077del XP_024301921.1:p.Arg359SerfsTer?
XM_024446154.1:c.657del XP_024301922.1:p.Arg219SerfsTer?
XM_024446155.1:c.270del XP_024301923.1:p.Arg90SerfsTer?
XM_024446156.1:c.270del XP_024301924.1:p.Arg90SerfsTer?
XM_024446158.1:c.270del XP_024301926.1:p.Arg90SerfsTer?
XM_024446159.1:c.21del XP_024301927.1:p.Arg7SerfsTer?
XM_024446160.1:c.1077del XP_024301928.1:p.Arg359SerfsTer?
XM_024446161.1:c.1077del XP_024301929.1:p.Arg359SerfsTer?
XM_024446162.1:c.-2919del XP_024301930.1:n.-2919del
NM_022455.5:c.1077del MANE Select NP_071900.2:p.Arg359SerfsTer?
NM_172349.3:c.270del NP_758859.1:p.Arg90SerfsTer?