Canonical Allele Identifier: CA294878

Gene: NSD1

Linked Data

• ClinVar Variation Id: 159328
• ClinVar RCV Id: RCV000760278 ; RCV003231228
• dbSNP Id: rs587784115
• MyVariant Identifiers: chr5:g.176671272G>A (hg19) ; chr5:g.177244271G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177244271G>A , CM000667.2:g.177244271G>A	GRCh38
NC_000005.9:g.176671272G>A , CM000667.1:g.176671272G>A	GRCh37
NC_000005.8:g.176603878G>A	NCBI36
NG_009821.1:g.116193G>A , LRG_512:g.116193G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508896.7:c.3505+1G>A	ENSP00000423372.3:n.3505+1G>A
ENST00000347982.9:c.3505+1G>A	ENSP00000343209.5:n.3505+1G>A
ENST00000354179.9:c.3505+1G>A	ENSP00000346111.5:n.3505+1G>A
ENST00000685206.1:n.3961+1G>A
ENST00000686993.1:c.3505+1G>A	ENSP00000510020.1:n.3505+1G>A
ENST00000687453.1:c.4069+1G>A	ENSP00000508426.1:n.4069+1G>A
ENST00000688613.1:n.3775+1G>A
ENST00000689326.1:c.*123+1G>A	ENSP00000509594.1:n.*123+1G>A
ENST00000689345.1:c.3505+1G>A	ENSP00000509711.1:n.3505+1G>A
ENST00000689549.1:n.4525+1G>A
ENST00000439151.7:c.4378+1G>A MANE Select	ENSP00000395929.2:n.4378+1G>A
ENST00000347982.8:c.3571+1G>A	ENSP00000343209.4:n.3571+1G>A
ENST00000354179.8:c.3571+1G>A	ENSP00000346111.4:n.3571+1G>A
ENST00000439151.6:c.4378+1G>A	ENSP00000395929.2:n.4378+1G>A
NM_022455.4:c.4378+1G>A , LRG_512t1:c.4378+1G>A	NP_071900.2:n.4378+1G>A
NM_172349.2:c.3571+1G>A	NP_758859.1:n.3571+1G>A
XM_005265959.1:c.4378+1G>A	XP_005266016.1:n.4378+1G>A
XM_005265960.1:c.3571+1G>A	XP_005266017.1:n.3571+1G>A
XM_005265961.1:c.3571+1G>A	XP_005266018.1:n.3571+1G>A
XM_011534610.1:c.4378+1G>A	XP_011532912.1:n.4378+1G>A
XM_011534611.1:c.4378+1G>A	XP_011532913.1:n.4378+1G>A
XM_011534612.1:c.3958+1G>A	XP_011532914.1:n.3958+1G>A
XM_011534613.1:c.3322+1G>A	XP_011532915.1:n.3322+1G>A
XM_011534614.1:c.4378+1G>A	XP_011532916.1:n.4378+1G>A
XM_011534615.1:c.4378+1G>A	XP_011532917.1:n.4378+1G>A
XM_011534617.1:c.112+1G>A	XP_011532919.1:n.112+1G>A
NM_001365684.1:c.3571+1G>A	NP_001352613.1:n.3571+1G>A
XM_024446150.1:c.4378+1G>A	XP_024301918.1:n.4378+1G>A
XM_024446151.1:c.4378+1G>A	XP_024301919.1:n.4378+1G>A
XM_024446152.1:c.4378+1G>A	XP_024301920.1:n.4378+1G>A
XM_024446153.1:c.4378+1G>A	XP_024301921.1:n.4378+1G>A
XM_024446154.1:c.3958+1G>A	XP_024301922.1:n.3958+1G>A
XM_024446155.1:c.3571+1G>A	XP_024301923.1:n.3571+1G>A
XM_024446156.1:c.3571+1G>A	XP_024301924.1:n.3571+1G>A
XM_024446158.1:c.3571+1G>A	XP_024301926.1:n.3571+1G>A
XM_024446159.1:c.3322+1G>A	XP_024301927.1:n.3322+1G>A
XM_024446160.1:c.4378+1G>A	XP_024301928.1:n.4378+1G>A
XM_024446161.1:c.4378+1G>A	XP_024301929.1:n.4378+1G>A
XM_024446162.1:c.112+1G>A	XP_024301930.1:n.112+1G>A
NM_022455.5:c.4378+1G>A MANE Select	NP_071900.2:n.4378+1G>A
NM_172349.3:c.3571+1G>A	NP_758859.1:n.3571+1G>A