Canonical Allele Identifier: CA3578032
Gene: NSD1 HGNC NCBI

Linked Data

dbSNP Id: rs774102871

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177294075T>C , CM000667.2:g.177294075T>C GRCh38
NC_000005.9:g.176721076T>C , CM000667.1:g.176721076T>C GRCh37
NC_000005.8:g.176653682T>C NCBI36
NG_009821.1:g.165997T>C , LRG_512:g.165997T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000508896.7:c.5834T>C ENSP00000423372.3:p.Leu1945Pro
ENST00000347982.9:c.5834T>C ENSP00000343209.5:p.Leu1945Pro
ENST00000354179.9:c.5834T>C ENSP00000346111.5:p.Leu1945Pro
ENST00000503056.6:c.1349T>C ENSP00000424024.2:p.Leu450Pro
ENST00000508029.6:c.1349T>C ENSP00000425120.2:p.Leu450Pro
ENST00000685206.1:n.6290T>C
ENST00000686385.1:n.1123T>C
ENST00000686993.1:c.5834T>C ENSP00000510020.1:p.Leu1945Pro
ENST00000687453.1:c.6398T>C ENSP00000508426.1:p.Leu2133Pro
ENST00000688613.1:n.6104T>C
ENST00000689345.1:c.5834T>C ENSP00000509711.1:p.Leu1945Pro
ENST00000439151.7:c.6707T>C MANE Select ENSP00000395929.2:p.Leu2236Pro
ENST00000347982.8:c.5900T>C ENSP00000343209.4:p.Leu1967Pro
ENST00000354179.8:c.5900T>C ENSP00000346111.4:p.Leu1967Pro
ENST00000439151.6:c.6707T>C ENSP00000395929.2:p.Leu2236Pro
NM_022455.4:c.6707T>C , LRG_512t1:c.6707T>C NP_071900.2:p.Leu2236Pro
NM_172349.2:c.5900T>C NP_758859.1:p.Leu1967Pro
XM_005265959.1:c.6707T>C XP_005266016.1:p.Leu2236Pro
XM_005265960.1:c.5900T>C XP_005266017.1:p.Leu1967Pro
XM_005265961.1:c.5900T>C XP_005266018.1:p.Leu1967Pro
XM_005265962.3:c.2201T>C XP_005266019.1:p.Leu734Pro
XM_011534610.1:c.6707T>C XP_011532912.1:p.Leu2236Pro
XM_011534611.1:c.6707T>C XP_011532913.1:p.Leu2236Pro
XM_011534612.1:c.6287T>C XP_011532914.1:p.Leu2096Pro
XM_011534613.1:c.5651T>C XP_011532915.1:p.Leu1884Pro
XM_011534617.1:c.2441T>C XP_011532919.1:p.Leu814Pro
NM_001365684.1:c.5900T>C NP_001352613.1:p.Leu1967Pro
XM_024446150.1:c.6707T>C XP_024301918.1:p.Leu2236Pro
XM_024446151.1:c.6707T>C XP_024301919.1:p.Leu2236Pro
XM_024446152.1:c.6707T>C XP_024301920.1:p.Leu2236Pro
XM_024446153.1:c.6707T>C XP_024301921.1:p.Leu2236Pro
XM_024446154.1:c.6287T>C XP_024301922.1:p.Leu2096Pro
XM_024446155.1:c.5900T>C XP_024301923.1:p.Leu1967Pro
XM_024446156.1:c.5900T>C XP_024301924.1:p.Leu1967Pro
XM_024446158.1:c.5900T>C XP_024301926.1:p.Leu1967Pro
XM_024446159.1:c.5651T>C XP_024301927.1:p.Leu1884Pro
XM_024446162.1:c.2441T>C XP_024301930.1:p.Leu814Pro
XM_024446163.1:c.2201T>C XP_024301931.1:p.Leu734Pro
NM_022455.5:c.6707T>C MANE Select NP_071900.2:p.Leu2236Pro
NM_172349.3:c.5900T>C NP_758859.1:p.Leu1967Pro