Canonical Allele Identifier: CA362303016
Gene: NSD1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177260078A>T , CM000667.2:g.177260078A>T GRCh38
NC_000005.9:g.176687079A>T , CM000667.1:g.176687079A>T GRCh37
NC_000005.8:g.176619685A>T NCBI36
NG_009821.1:g.132000A>T , LRG_512:g.132000A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000508896.7:c.4183A>T ENSP00000423372.3:p.Ser1395Cys
ENST00000347982.9:c.4183A>T ENSP00000343209.5:p.Ser1395Cys
ENST00000354179.9:c.4183A>T ENSP00000346111.5:p.Ser1395Cys
ENST00000685206.1:n.4639A>T
ENST00000686993.1:c.4183A>T ENSP00000510020.1:p.Ser1395Cys
ENST00000687453.1:c.4747A>T ENSP00000508426.1:p.Ser1583Cys
ENST00000688613.1:n.4453A>T
ENST00000689345.1:c.4183A>T ENSP00000509711.1:p.Ser1395Cys
ENST00000689549.1:n.5203A>T
ENST00000439151.7:c.5056A>T MANE Select ENSP00000395929.2:p.Ser1686Cys
ENST00000347982.8:c.4249A>T ENSP00000343209.4:p.Ser1417Cys
ENST00000354179.8:c.4249A>T ENSP00000346111.4:p.Ser1417Cys
ENST00000439151.6:c.5056A>T ENSP00000395929.2:p.Ser1686Cys
NM_022455.4:c.5056A>T , LRG_512t1:c.5056A>T NP_071900.2:p.Ser1686Cys
NM_172349.2:c.4249A>T NP_758859.1:p.Ser1417Cys
XM_005265959.1:c.5056A>T XP_005266016.1:p.Ser1686Cys
XM_005265960.1:c.4249A>T XP_005266017.1:p.Ser1417Cys
XM_005265961.1:c.4249A>T XP_005266018.1:p.Ser1417Cys
XM_005265962.3:c.550A>T XP_005266019.1:p.Ser184Cys
XM_011534610.1:c.5056A>T XP_011532912.1:p.Ser1686Cys
XM_011534611.1:c.5056A>T XP_011532913.1:p.Ser1686Cys
XM_011534612.1:c.4636A>T XP_011532914.1:p.Ser1546Cys
XM_011534613.1:c.4000A>T XP_011532915.1:p.Ser1334Cys
XM_011534614.1:c.5056A>T XP_011532916.1:p.Ser1686Cys
XM_011534617.1:c.790A>T XP_011532919.1:p.Ser264Cys
NM_001365684.1:c.4249A>T NP_001352613.1:p.Ser1417Cys
XM_024446150.1:c.5056A>T XP_024301918.1:p.Ser1686Cys
XM_024446151.1:c.5056A>T XP_024301919.1:p.Ser1686Cys
XM_024446152.1:c.5056A>T XP_024301920.1:p.Ser1686Cys
XM_024446153.1:c.5056A>T XP_024301921.1:p.Ser1686Cys
XM_024446154.1:c.4636A>T XP_024301922.1:p.Ser1546Cys
XM_024446155.1:c.4249A>T XP_024301923.1:p.Ser1417Cys
XM_024446156.1:c.4249A>T XP_024301924.1:p.Ser1417Cys
XM_024446158.1:c.4249A>T XP_024301926.1:p.Ser1417Cys
XM_024446159.1:c.4000A>T XP_024301927.1:p.Ser1334Cys
XM_024446160.1:c.5056A>T XP_024301928.1:p.Ser1686Cys
XM_024446162.1:c.790A>T XP_024301930.1:p.Ser264Cys
XM_024446163.1:c.550A>T XP_024301931.1:p.Ser184Cys
NM_022455.5:c.5056A>T MANE Select NP_071900.2:p.Ser1686Cys
NM_172349.3:c.4249A>T NP_758859.1:p.Ser1417Cys