Canonical Allele Identifier: CA1603543533
Gene: NSD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177273728C= , CM000667.2:g.177273728C= GRCh38
NC_000005.9:g.176700729C= , CM000667.1:g.176700729C= GRCh37
NC_000005.8:g.176633335C= NCBI36
NG_009821.1:g.145650C= , LRG_512:g.145650C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000508896.7:c.4693C= ENSP00000423372.3:p.Gln1565=
ENST00000347982.9:c.4693C= ENSP00000343209.5:p.Gln1565=
ENST00000354179.9:c.4693C= ENSP00000346111.5:p.Gln1565=
ENST00000503056.6:c.208C= ENSP00000424024.2:p.Gln70=
ENST00000508029.6:c.208C= ENSP00000425120.2:p.Gln70=
ENST00000685206.1:n.5149C=
ENST00000686993.1:c.4693C= ENSP00000510020.1:p.Gln1565=
ENST00000687095.1:n.315C=
ENST00000687453.1:c.5257C= ENSP00000508426.1:p.Gln1753=
ENST00000688613.1:n.4963C=
ENST00000689345.1:c.4693C= ENSP00000509711.1:p.Gln1565=
ENST00000689549.1:n.5713C=
ENST00000692024.1:n.2485C=
ENST00000439151.7:c.5566C= MANE Select ENSP00000395929.2:p.Gln1856=
ENST00000347982.8:c.4759C= ENSP00000343209.4:p.Gln1587=
ENST00000354179.8:c.4759C= ENSP00000346111.4:p.Gln1587=
ENST00000439151.6:c.5566C= ENSP00000395929.2:p.Gln1856=
ENST00000503056.5:c.208C= ENSP00000424024.1:p.Gln70=
NM_022455.4:c.5566C= , LRG_512t1:c.5566C= NP_071900.2:p.Gln1856=
NM_172349.2:c.4759C= NP_758859.1:p.Gln1587=
XM_005265959.1:c.5566C= XP_005266016.1:p.Gln1856=
XM_005265960.1:c.4759C= XP_005266017.1:p.Gln1587=
XM_005265961.1:c.4759C= XP_005266018.1:p.Gln1587=
XM_005265962.3:c.1060C= XP_005266019.1:p.Gln354=
XM_011534610.1:c.5566C= XP_011532912.1:p.Gln1856=
XM_011534611.1:c.5566C= XP_011532913.1:p.Gln1856=
XM_011534612.1:c.5146C= XP_011532914.1:p.Gln1716=
XM_011534613.1:c.4510C= XP_011532915.1:p.Gln1504=
XM_011534617.1:c.1300C= XP_011532919.1:p.Gln434=
NM_001365684.1:c.4759C= NP_001352613.1:p.Gln1587=
XM_024446150.1:c.5566C= XP_024301918.1:p.Gln1856=
XM_024446151.1:c.5566C= XP_024301919.1:p.Gln1856=
XM_024446152.1:c.5566C= XP_024301920.1:p.Gln1856=
XM_024446153.1:c.5566C= XP_024301921.1:p.Gln1856=
XM_024446154.1:c.5146C= XP_024301922.1:p.Gln1716=
XM_024446155.1:c.4759C= XP_024301923.1:p.Gln1587=
XM_024446156.1:c.4759C= XP_024301924.1:p.Gln1587=
XM_024446158.1:c.4759C= XP_024301926.1:p.Gln1587=
XM_024446159.1:c.4510C= XP_024301927.1:p.Gln1504=
XM_024446162.1:c.1300C= XP_024301930.1:p.Gln434=
XM_024446163.1:c.1060C= XP_024301931.1:p.Gln354=
NM_022455.5:c.5566C= MANE Select NP_071900.2:p.Gln1856=
NM_172349.3:c.4759C= NP_758859.1:p.Gln1587=