Canonical Allele Identifier: CA1603535611
Gene: NSD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177294015G= , CM000667.2:g.177294015G= GRCh38
NC_000005.9:g.176721016G= , CM000667.1:g.176721016G= GRCh37
NC_000005.8:g.176653622G= NCBI36
NG_009821.1:g.165937G= , LRG_512:g.165937G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000508896.7:c.5774G= ENSP00000423372.3:p.Gly1925=
ENST00000347982.9:c.5774G= ENSP00000343209.5:p.Gly1925=
ENST00000354179.9:c.5774G= ENSP00000346111.5:p.Gly1925=
ENST00000503056.6:c.1289G= ENSP00000424024.2:p.Gly430=
ENST00000508029.6:c.1289G= ENSP00000425120.2:p.Gly430=
ENST00000685206.1:n.6230G=
ENST00000686385.1:n.1063G=
ENST00000686993.1:c.5774G= ENSP00000510020.1:p.Gly1925=
ENST00000687453.1:c.6338G= ENSP00000508426.1:p.Gly2113=
ENST00000688613.1:n.6044G=
ENST00000689345.1:c.5774G= ENSP00000509711.1:p.Gly1925=
ENST00000439151.7:c.6647G= MANE Select ENSP00000395929.2:p.Gly2216=
ENST00000347982.8:c.5840G= ENSP00000343209.4:p.Gly1947=
ENST00000354179.8:c.5840G= ENSP00000346111.4:p.Gly1947=
ENST00000439151.6:c.6647G= ENSP00000395929.2:p.Gly2216=
NM_022455.4:c.6647G= , LRG_512t1:c.6647G= NP_071900.2:p.Gly2216=
NM_172349.2:c.5840G= NP_758859.1:p.Gly1947=
XM_005265959.1:c.6647G= XP_005266016.1:p.Gly2216=
XM_005265960.1:c.5840G= XP_005266017.1:p.Gly1947=
XM_005265961.1:c.5840G= XP_005266018.1:p.Gly1947=
XM_005265962.3:c.2141G= XP_005266019.1:p.Gly714=
XM_011534610.1:c.6647G= XP_011532912.1:p.Gly2216=
XM_011534611.1:c.6647G= XP_011532913.1:p.Gly2216=
XM_011534612.1:c.6227G= XP_011532914.1:p.Gly2076=
XM_011534613.1:c.5591G= XP_011532915.1:p.Gly1864=
XM_011534617.1:c.2381G= XP_011532919.1:p.Gly794=
NM_001365684.1:c.5840G= NP_001352613.1:p.Gly1947=
XM_024446150.1:c.6647G= XP_024301918.1:p.Gly2216=
XM_024446151.1:c.6647G= XP_024301919.1:p.Gly2216=
XM_024446152.1:c.6647G= XP_024301920.1:p.Gly2216=
XM_024446153.1:c.6647G= XP_024301921.1:p.Gly2216=
XM_024446154.1:c.6227G= XP_024301922.1:p.Gly2076=
XM_024446155.1:c.5840G= XP_024301923.1:p.Gly1947=
XM_024446156.1:c.5840G= XP_024301924.1:p.Gly1947=
XM_024446158.1:c.5840G= XP_024301926.1:p.Gly1947=
XM_024446159.1:c.5591G= XP_024301927.1:p.Gly1864=
XM_024446162.1:c.2381G= XP_024301930.1:p.Gly794=
XM_024446163.1:c.2141G= XP_024301931.1:p.Gly714=
NM_022455.5:c.6647G= MANE Select NP_071900.2:p.Gly2216=
NM_172349.3:c.5840G= NP_758859.1:p.Gly1947=