Canonical Allele Identifier: CA564898907
Gene: NSD1 HGNC NCBI

Linked Data

dbSNP Id: rs1252292122

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177257165dup , CM000667.2:g.177257165dup GRCh38
NC_000005.9:g.176684166dup , CM000667.1:g.176684166dup GRCh37
NC_000005.8:g.176616772dup NCBI36
NG_009821.1:g.129087dup , LRG_512:g.129087dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000508896.7:c.4093+14dup ENSP00000423372.3:n.4093+14dup
ENST00000347982.9:c.4093+14dup ENSP00000343209.5:n.4093+14dup
ENST00000354179.9:c.4093+14dup ENSP00000346111.5:n.4093+14dup
ENST00000685206.1:n.4549+14dup
ENST00000686993.1:c.4093+14dup ENSP00000510020.1:n.4093+14dup
ENST00000687453.1:c.4657+14dup ENSP00000508426.1:n.4657+14dup
ENST00000688613.1:n.4363+14dup
ENST00000689345.1:c.4093+14dup ENSP00000509711.1:n.4093+14dup
ENST00000689549.1:n.5113+14dup
ENST00000439151.7:c.4966+14dup MANE Select ENSP00000395929.2:n.4966+14dup
ENST00000347982.8:c.4159+14dup ENSP00000343209.4:n.4159+14dup
ENST00000354179.8:c.4159+14dup ENSP00000346111.4:n.4159+14dup
ENST00000439151.6:c.4966+14dup ENSP00000395929.2:n.4966+14dup
NM_022455.4:c.4966+14dup , LRG_512t1:c.4966+14dup NP_071900.2:n.4966+14dup
NM_172349.2:c.4159+14dup NP_758859.1:n.4159+14dup
XM_005265959.1:c.4966+14dup XP_005266016.1:n.4966+14dup
XM_005265960.1:c.4159+14dup XP_005266017.1:n.4159+14dup
XM_005265961.1:c.4159+14dup XP_005266018.1:n.4159+14dup
XM_005265962.3:c.460+14dup XP_005266019.1:n.460+14dup
XM_011534610.1:c.4966+14dup XP_011532912.1:n.4966+14dup
XM_011534611.1:c.4966+14dup XP_011532913.1:n.4966+14dup
XM_011534612.1:c.4546+14dup XP_011532914.1:n.4546+14dup
XM_011534613.1:c.3910+14dup XP_011532915.1:n.3910+14dup
XM_011534614.1:c.4966+14dup XP_011532916.1:n.4966+14dup
XM_011534617.1:c.700+14dup XP_011532919.1:n.700+14dup
NM_001365684.1:c.4159+14dup NP_001352613.1:n.4159+14dup
XM_024446150.1:c.4966+14dup XP_024301918.1:n.4966+14dup
XM_024446151.1:c.4966+14dup XP_024301919.1:n.4966+14dup
XM_024446152.1:c.4966+14dup XP_024301920.1:n.4966+14dup
XM_024446153.1:c.4966+14dup XP_024301921.1:n.4966+14dup
XM_024446154.1:c.4546+14dup XP_024301922.1:n.4546+14dup
XM_024446155.1:c.4159+14dup XP_024301923.1:n.4159+14dup
XM_024446156.1:c.4159+14dup XP_024301924.1:n.4159+14dup
XM_024446158.1:c.4159+14dup XP_024301926.1:n.4159+14dup
XM_024446159.1:c.3910+14dup XP_024301927.1:n.3910+14dup
XM_024446160.1:c.4966+14dup XP_024301928.1:n.4966+14dup
XM_024446162.1:c.700+14dup XP_024301930.1:n.700+14dup
XM_024446163.1:c.460+14dup XP_024301931.1:n.460+14dup
NM_022455.5:c.4966+14dup MANE Select NP_071900.2:n.4966+14dup
NM_172349.3:c.4159+14dup NP_758859.1:n.4159+14dup