Canonical Allele Identifier: CA16618184

Gene: NSD1

Linked Data

• ClinVar Variation Id: 421325
• ClinVar RCV Id: RCV000481475
• dbSNP Id: rs1064795059
• MyVariant Identifiers: chr5:g.176709476T>C (hg19) ; chr5:g.177282475T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177282475T>C , CM000667.2:g.177282475T>C	GRCh38
NC_000005.9:g.176709476T>C , CM000667.1:g.176709476T>C	GRCh37
NC_000005.8:g.176642082T>C	NCBI36
NG_009821.1:g.154397T>C , LRG_512:g.154397T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508896.7:c.5030T>C	ENSP00000423372.3:p.Val1677Ala
ENST00000347982.9:c.5030T>C	ENSP00000343209.5:p.Val1677Ala
ENST00000354179.9:c.5030T>C	ENSP00000346111.5:p.Val1677Ala
ENST00000503056.6:c.545T>C	ENSP00000424024.2:p.Val182Ala
ENST00000508029.6:c.545T>C	ENSP00000425120.2:p.Val182Ala
ENST00000685206.1:n.5486T>C
ENST00000686993.1:c.5030T>C	ENSP00000510020.1:p.Val1677Ala
ENST00000687453.1:c.5594T>C	ENSP00000508426.1:p.Val1865Ala
ENST00000688613.1:n.5300T>C
ENST00000689345.1:c.5030T>C	ENSP00000509711.1:p.Val1677Ala
ENST00000689549.1:n.6050T>C
ENST00000692024.1:n.4452T>C
ENST00000439151.7:c.5903T>C MANE Select	ENSP00000395929.2:p.Val1968Ala
ENST00000347982.8:c.5096T>C	ENSP00000343209.4:p.Val1699Ala
ENST00000354179.8:c.5096T>C	ENSP00000346111.4:p.Val1699Ala
ENST00000439151.6:c.5903T>C	ENSP00000395929.2:p.Val1968Ala
NM_022455.4:c.5903T>C , LRG_512t1:c.5903T>C	NP_071900.2:p.Val1968Ala
NM_172349.2:c.5096T>C	NP_758859.1:p.Val1699Ala
XM_005265959.1:c.5903T>C	XP_005266016.1:p.Val1968Ala
XM_005265960.1:c.5096T>C	XP_005266017.1:p.Val1699Ala
XM_005265961.1:c.5096T>C	XP_005266018.1:p.Val1699Ala
XM_005265962.3:c.1397T>C	XP_005266019.1:p.Val466Ala
XM_011534610.1:c.5903T>C	XP_011532912.1:p.Val1968Ala
XM_011534611.1:c.5903T>C	XP_011532913.1:p.Val1968Ala
XM_011534612.1:c.5483T>C	XP_011532914.1:p.Val1828Ala
XM_011534613.1:c.4847T>C	XP_011532915.1:p.Val1616Ala
XM_011534617.1:c.1637T>C	XP_011532919.1:p.Val546Ala
NM_001365684.1:c.5096T>C	NP_001352613.1:p.Val1699Ala
XM_024446150.1:c.5903T>C	XP_024301918.1:p.Val1968Ala
XM_024446151.1:c.5903T>C	XP_024301919.1:p.Val1968Ala
XM_024446152.1:c.5903T>C	XP_024301920.1:p.Val1968Ala
XM_024446153.1:c.5903T>C	XP_024301921.1:p.Val1968Ala
XM_024446154.1:c.5483T>C	XP_024301922.1:p.Val1828Ala
XM_024446155.1:c.5096T>C	XP_024301923.1:p.Val1699Ala
XM_024446156.1:c.5096T>C	XP_024301924.1:p.Val1699Ala
XM_024446158.1:c.5096T>C	XP_024301926.1:p.Val1699Ala
XM_024446159.1:c.4847T>C	XP_024301927.1:p.Val1616Ala
XM_024446162.1:c.1637T>C	XP_024301930.1:p.Val546Ala
XM_024446163.1:c.1397T>C	XP_024301931.1:p.Val466Ala
NM_022455.5:c.5903T>C MANE Select	NP_071900.2:p.Val1968Ala
NM_172349.3:c.5096T>C	NP_758859.1:p.Val1699Ala