Canonical Allele Identifier: CA1603543544
Gene: NSD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177273743C= , CM000667.2:g.177273743C= GRCh38
NC_000005.9:g.176700744C= , CM000667.1:g.176700744C= GRCh37
NC_000005.8:g.176633350C= NCBI36
NG_009821.1:g.145665C= , LRG_512:g.145665C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000508896.7:c.4708C= ENSP00000423372.3:p.Arg1570=
ENST00000347982.9:c.4708C= ENSP00000343209.5:p.Arg1570=
ENST00000354179.9:c.4708C= ENSP00000346111.5:p.Arg1570=
ENST00000503056.6:c.223C= ENSP00000424024.2:p.Arg75=
ENST00000508029.6:c.223C= ENSP00000425120.2:p.Arg75=
ENST00000685206.1:n.5164C=
ENST00000686993.1:c.4708C= ENSP00000510020.1:p.Arg1570=
ENST00000687095.1:n.330C=
ENST00000687453.1:c.5272C= ENSP00000508426.1:p.Arg1758=
ENST00000688613.1:n.4978C=
ENST00000689345.1:c.4708C= ENSP00000509711.1:p.Arg1570=
ENST00000689549.1:n.5728C=
ENST00000692024.1:n.2500C=
ENST00000439151.7:c.5581C= MANE Select ENSP00000395929.2:p.Arg1861=
ENST00000347982.8:c.4774C= ENSP00000343209.4:p.Arg1592=
ENST00000354179.8:c.4774C= ENSP00000346111.4:p.Arg1592=
ENST00000439151.6:c.5581C= ENSP00000395929.2:p.Arg1861=
ENST00000503056.5:c.223C= ENSP00000424024.1:p.Arg75=
NM_022455.4:c.5581C= , LRG_512t1:c.5581C= NP_071900.2:p.Arg1861=
NM_172349.2:c.4774C= NP_758859.1:p.Arg1592=
XM_005265959.1:c.5581C= XP_005266016.1:p.Arg1861=
XM_005265960.1:c.4774C= XP_005266017.1:p.Arg1592=
XM_005265961.1:c.4774C= XP_005266018.1:p.Arg1592=
XM_005265962.3:c.1075C= XP_005266019.1:p.Arg359=
XM_011534610.1:c.5581C= XP_011532912.1:p.Arg1861=
XM_011534611.1:c.5581C= XP_011532913.1:p.Arg1861=
XM_011534612.1:c.5161C= XP_011532914.1:p.Arg1721=
XM_011534613.1:c.4525C= XP_011532915.1:p.Arg1509=
XM_011534617.1:c.1315C= XP_011532919.1:p.Arg439=
NM_001365684.1:c.4774C= NP_001352613.1:p.Arg1592=
XM_024446150.1:c.5581C= XP_024301918.1:p.Arg1861=
XM_024446151.1:c.5581C= XP_024301919.1:p.Arg1861=
XM_024446152.1:c.5581C= XP_024301920.1:p.Arg1861=
XM_024446153.1:c.5581C= XP_024301921.1:p.Arg1861=
XM_024446154.1:c.5161C= XP_024301922.1:p.Arg1721=
XM_024446155.1:c.4774C= XP_024301923.1:p.Arg1592=
XM_024446156.1:c.4774C= XP_024301924.1:p.Arg1592=
XM_024446158.1:c.4774C= XP_024301926.1:p.Arg1592=
XM_024446159.1:c.4525C= XP_024301927.1:p.Arg1509=
XM_024446162.1:c.1315C= XP_024301930.1:p.Arg439=
XM_024446163.1:c.1075C= XP_024301931.1:p.Arg359=
NM_022455.5:c.5581C= MANE Select NP_071900.2:p.Arg1861=
NM_172349.3:c.4774C= NP_758859.1:p.Arg1592=