Canonical Allele Identifier: CA10588401

Gene: NSD1

Linked Data

• ClinVar Variation Id: 265497
• ClinVar RCV Id: RCV000255457 ; RCV003231617
• dbSNP Id: rs886039579
• COSMIC: COSM4605652 ; COSM4605653
• MyVariant Identifiers: chr5:g.176707836G>T (hg19) ; chr5:g.177280835G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177280835G>T , CM000667.2:g.177280835G>T	GRCh38
NC_000005.9:g.176707836G>T , CM000667.1:g.176707836G>T	GRCh37
NC_000005.8:g.176640442G>T	NCBI36
NG_009821.1:g.152757G>T , LRG_512:g.152757G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508896.7:c.5019+1G>T	ENSP00000423372.3:n.5019+1G>T
ENST00000347982.9:c.5019+1G>T	ENSP00000343209.5:n.5019+1G>T
ENST00000354179.9:c.5019+1G>T	ENSP00000346111.5:n.5019+1G>T
ENST00000503056.6:c.534+1G>T	ENSP00000424024.2:n.534+1G>T
ENST00000508029.6:c.534+1G>T	ENSP00000425120.2:n.534+1G>T
ENST00000685206.1:n.5475+1G>T
ENST00000686993.1:c.5019+1G>T	ENSP00000510020.1:n.5019+1G>T
ENST00000687453.1:c.5583+1G>T	ENSP00000508426.1:n.5583+1G>T
ENST00000688613.1:n.5289+1G>T
ENST00000689345.1:c.5019+1G>T	ENSP00000509711.1:n.5019+1G>T
ENST00000689549.1:n.6039+1G>T
ENST00000692024.1:n.2812G>T
ENST00000439151.7:c.5892+1G>T MANE Select	ENSP00000395929.2:n.5892+1G>T
ENST00000347982.8:c.5085+1G>T	ENSP00000343209.4:n.5085+1G>T
ENST00000354179.8:c.5085+1G>T	ENSP00000346111.4:n.5085+1G>T
ENST00000439151.6:c.5892+1G>T	ENSP00000395929.2:n.5892+1G>T
NM_022455.4:c.5892+1G>T , LRG_512t1:c.5892+1G>T	NP_071900.2:n.5892+1G>T
NM_172349.2:c.5085+1G>T	NP_758859.1:n.5085+1G>T
XM_005265959.1:c.5892+1G>T	XP_005266016.1:n.5892+1G>T
XM_005265960.1:c.5085+1G>T	XP_005266017.1:n.5085+1G>T
XM_005265961.1:c.5085+1G>T	XP_005266018.1:n.5085+1G>T
XM_005265962.3:c.1386+1G>T	XP_005266019.1:n.1386+1G>T
XM_011534610.1:c.5892+1G>T	XP_011532912.1:n.5892+1G>T
XM_011534611.1:c.5892+1G>T	XP_011532913.1:n.5892+1G>T
XM_011534612.1:c.5472+1G>T	XP_011532914.1:n.5472+1G>T
XM_011534613.1:c.4836+1G>T	XP_011532915.1:n.4836+1G>T
XM_011534617.1:c.1626+1G>T	XP_011532919.1:n.1626+1G>T
NM_001365684.1:c.5085+1G>T	NP_001352613.1:n.5085+1G>T
XM_024446150.1:c.5892+1G>T	XP_024301918.1:n.5892+1G>T
XM_024446151.1:c.5892+1G>T	XP_024301919.1:n.5892+1G>T
XM_024446152.1:c.5892+1G>T	XP_024301920.1:n.5892+1G>T
XM_024446153.1:c.5892+1G>T	XP_024301921.1:n.5892+1G>T
XM_024446154.1:c.5472+1G>T	XP_024301922.1:n.5472+1G>T
XM_024446155.1:c.5085+1G>T	XP_024301923.1:n.5085+1G>T
XM_024446156.1:c.5085+1G>T	XP_024301924.1:n.5085+1G>T
XM_024446158.1:c.5085+1G>T	XP_024301926.1:n.5085+1G>T
XM_024446159.1:c.4836+1G>T	XP_024301927.1:n.4836+1G>T
XM_024446162.1:c.1626+1G>T	XP_024301930.1:n.1626+1G>T
XM_024446163.1:c.1386+1G>T	XP_024301931.1:n.1386+1G>T
NM_022455.5:c.5892+1G>T MANE Select	NP_071900.2:n.5892+1G>T
NM_172349.3:c.5085+1G>T	NP_758859.1:n.5085+1G>T