Canonical Allele Identifier: CA362302845

Gene: NSD1

Linked Data

• dbSNP Id: rs1697168968
• COSMIC: COSM5039403 ; COSM5039404
• MyVariant Identifiers: chr5:g.176687049G>A (hg19) ; chr5:g.177260048G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177260048G>A , CM000667.2:g.177260048G>A	GRCh38
NC_000005.9:g.176687049G>A , CM000667.1:g.176687049G>A	GRCh37
NC_000005.8:g.176619655G>A	NCBI36
NG_009821.1:g.131970G>A , LRG_512:g.131970G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508896.7:c.4153G>A	ENSP00000423372.3:p.Ala1385Thr
ENST00000347982.9:c.4153G>A	ENSP00000343209.5:p.Ala1385Thr
ENST00000354179.9:c.4153G>A	ENSP00000346111.5:p.Ala1385Thr
ENST00000685206.1:n.4609G>A
ENST00000686993.1:c.4153G>A	ENSP00000510020.1:p.Ala1385Thr
ENST00000687453.1:c.4717G>A	ENSP00000508426.1:p.Ala1573Thr
ENST00000688613.1:n.4423G>A
ENST00000689345.1:c.4153G>A	ENSP00000509711.1:p.Ala1385Thr
ENST00000689549.1:n.5173G>A
ENST00000439151.7:c.5026G>A MANE Select	ENSP00000395929.2:p.Ala1676Thr
ENST00000347982.8:c.4219G>A	ENSP00000343209.4:p.Ala1407Thr
ENST00000354179.8:c.4219G>A	ENSP00000346111.4:p.Ala1407Thr
ENST00000439151.6:c.5026G>A	ENSP00000395929.2:p.Ala1676Thr
NM_022455.4:c.5026G>A , LRG_512t1:c.5026G>A	NP_071900.2:p.Ala1676Thr
NM_172349.2:c.4219G>A	NP_758859.1:p.Ala1407Thr
XM_005265959.1:c.5026G>A	XP_005266016.1:p.Ala1676Thr
XM_005265960.1:c.4219G>A	XP_005266017.1:p.Ala1407Thr
XM_005265961.1:c.4219G>A	XP_005266018.1:p.Ala1407Thr
XM_005265962.3:c.520G>A	XP_005266019.1:p.Ala174Thr
XM_011534610.1:c.5026G>A	XP_011532912.1:p.Ala1676Thr
XM_011534611.1:c.5026G>A	XP_011532913.1:p.Ala1676Thr
XM_011534612.1:c.4606G>A	XP_011532914.1:p.Ala1536Thr
XM_011534613.1:c.3970G>A	XP_011532915.1:p.Ala1324Thr
XM_011534614.1:c.5026G>A	XP_011532916.1:p.Ala1676Thr
XM_011534617.1:c.760G>A	XP_011532919.1:p.Ala254Thr
NM_001365684.1:c.4219G>A	NP_001352613.1:p.Ala1407Thr
XM_024446150.1:c.5026G>A	XP_024301918.1:p.Ala1676Thr
XM_024446151.1:c.5026G>A	XP_024301919.1:p.Ala1676Thr
XM_024446152.1:c.5026G>A	XP_024301920.1:p.Ala1676Thr
XM_024446153.1:c.5026G>A	XP_024301921.1:p.Ala1676Thr
XM_024446154.1:c.4606G>A	XP_024301922.1:p.Ala1536Thr
XM_024446155.1:c.4219G>A	XP_024301923.1:p.Ala1407Thr
XM_024446156.1:c.4219G>A	XP_024301924.1:p.Ala1407Thr
XM_024446158.1:c.4219G>A	XP_024301926.1:p.Ala1407Thr
XM_024446159.1:c.3970G>A	XP_024301927.1:p.Ala1324Thr
XM_024446160.1:c.5026G>A	XP_024301928.1:p.Ala1676Thr
XM_024446162.1:c.760G>A	XP_024301930.1:p.Ala254Thr
XM_024446163.1:c.520G>A	XP_024301931.1:p.Ala174Thr
NM_022455.5:c.5026G>A MANE Select	NP_071900.2:p.Ala1676Thr
NM_172349.3:c.4219G>A	NP_758859.1:p.Ala1407Thr