Canonical Allele Identifier: CA295012
Gene: NSD1 HGNC NCBI

Linked Data

ClinVar Variation Id: 159391
dbSNP Id: rs587784170

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177282537C>T , CM000667.2:g.177282537C>T GRCh38
NC_000005.9:g.176709538C>T , CM000667.1:g.176709538C>T GRCh37
NC_000005.8:g.176642144C>T NCBI36
NG_009821.1:g.154459C>T , LRG_512:g.154459C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000508896.7:c.5092C>T ENSP00000423372.3:p.Gln1698Ter
ENST00000347982.9:c.5092C>T ENSP00000343209.5:p.Gln1698Ter
ENST00000354179.9:c.5092C>T ENSP00000346111.5:p.Gln1698Ter
ENST00000503056.6:c.607C>T ENSP00000424024.2:p.Gln203Ter
ENST00000508029.6:c.607C>T ENSP00000425120.2:p.Gln203Ter
ENST00000685206.1:n.5548C>T
ENST00000686993.1:c.5092C>T ENSP00000510020.1:p.Gln1698Ter
ENST00000687453.1:c.5656C>T ENSP00000508426.1:p.Gln1886Ter
ENST00000688613.1:n.5362C>T
ENST00000689345.1:c.5092C>T ENSP00000509711.1:p.Gln1698Ter
ENST00000689549.1:n.6112C>T
ENST00000692024.1:n.4514C>T
ENST00000439151.7:c.5965C>T MANE Select ENSP00000395929.2:p.Gln1989Ter
ENST00000347982.8:c.5158C>T ENSP00000343209.4:p.Gln1720Ter
ENST00000354179.8:c.5158C>T ENSP00000346111.4:p.Gln1720Ter
ENST00000439151.6:c.5965C>T ENSP00000395929.2:p.Gln1989Ter
NM_022455.4:c.5965C>T , LRG_512t1:c.5965C>T NP_071900.2:p.Gln1989Ter
NM_172349.2:c.5158C>T NP_758859.1:p.Gln1720Ter
XM_005265959.1:c.5965C>T XP_005266016.1:p.Gln1989Ter
XM_005265960.1:c.5158C>T XP_005266017.1:p.Gln1720Ter
XM_005265961.1:c.5158C>T XP_005266018.1:p.Gln1720Ter
XM_005265962.3:c.1459C>T XP_005266019.1:p.Gln487Ter
XM_011534610.1:c.5965C>T XP_011532912.1:p.Gln1989Ter
XM_011534611.1:c.5965C>T XP_011532913.1:p.Gln1989Ter
XM_011534612.1:c.5545C>T XP_011532914.1:p.Gln1849Ter
XM_011534613.1:c.4909C>T XP_011532915.1:p.Gln1637Ter
XM_011534617.1:c.1699C>T XP_011532919.1:p.Gln567Ter
NM_001365684.1:c.5158C>T NP_001352613.1:p.Gln1720Ter
XM_024446150.1:c.5965C>T XP_024301918.1:p.Gln1989Ter
XM_024446151.1:c.5965C>T XP_024301919.1:p.Gln1989Ter
XM_024446152.1:c.5965C>T XP_024301920.1:p.Gln1989Ter
XM_024446153.1:c.5965C>T XP_024301921.1:p.Gln1989Ter
XM_024446154.1:c.5545C>T XP_024301922.1:p.Gln1849Ter
XM_024446155.1:c.5158C>T XP_024301923.1:p.Gln1720Ter
XM_024446156.1:c.5158C>T XP_024301924.1:p.Gln1720Ter
XM_024446158.1:c.5158C>T XP_024301926.1:p.Gln1720Ter
XM_024446159.1:c.4909C>T XP_024301927.1:p.Gln1637Ter
XM_024446162.1:c.1699C>T XP_024301930.1:p.Gln567Ter
XM_024446163.1:c.1459C>T XP_024301931.1:p.Gln487Ter
NM_022455.5:c.5965C>T MANE Select NP_071900.2:p.Gln1989Ter
NM_172349.3:c.5158C>T NP_758859.1:p.Gln1720Ter