Canonical Allele Identifier: CA2711008711

Gene: NSD1

Linked Data

• dbSNP Id: rs2127262791

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177283779_177283786del , CM000667.2:g.177283779_177283786del	GRCh38
NC_000005.9:g.176710780_176710787del , CM000667.1:g.176710780_176710787del	GRCh37
NC_000005.8:g.176643386_176643393del	NCBI36
NG_009821.1:g.155701_155708del , LRG_512:g.155701_155708del

Transcript Alleles

HGVS	Amino-acid change
ENST00000508896.7:c.5137-8_5137-1del	ENSP00000423372.3:n.5137-8_5137-1del
ENST00000347982.9:c.5137-8_5137-1del	ENSP00000343209.5:n.5137-8_5137-1del
ENST00000354179.9:c.5137-8_5137-1del	ENSP00000346111.5:n.5137-8_5137-1del
ENST00000503056.6:c.652-8_652-1del	ENSP00000424024.2:n.652-8_652-1del
ENST00000508029.6:c.652-8_652-1del	ENSP00000425120.2:n.652-8_652-1del
ENST00000685206.1:n.5593-8_5593-1del
ENST00000686993.1:c.5137-8_5137-1del	ENSP00000510020.1:n.5137-8_5137-1del
ENST00000687453.1:c.5701-8_5701-1del	ENSP00000508426.1:n.5701-8_5701-1del
ENST00000688613.1:n.5407-8_5407-1del
ENST00000689345.1:c.5137-8_5137-1del	ENSP00000509711.1:n.5137-8_5137-1del
ENST00000689549.1:n.6157-8_6157-1del
ENST00000692024.1:n.4559-8_4559-1del
ENST00000439151.7:c.6010-8_6010-1del MANE Select	ENSP00000395929.2:n.6010-8_6010-1del
ENST00000347982.8:c.5203-8_5203-1del	ENSP00000343209.4:n.5203-8_5203-1del
ENST00000354179.8:c.5203-8_5203-1del	ENSP00000346111.4:n.5203-8_5203-1del
ENST00000439151.6:c.6010-8_6010-1del	ENSP00000395929.2:n.6010-8_6010-1del
NM_022455.4:c.6010-8_6010-1del , LRG_512t1:c.6010-8_6010-1del	NP_071900.2:n.6010-8_6010-1del
NM_172349.2:c.5203-8_5203-1del	NP_758859.1:n.5203-8_5203-1del
XM_005265959.1:c.6010-8_6010-1del	XP_005266016.1:n.6010-8_6010-1del
XM_005265960.1:c.5203-8_5203-1del	XP_005266017.1:n.5203-8_5203-1del
XM_005265961.1:c.5203-8_5203-1del	XP_005266018.1:n.5203-8_5203-1del
XM_005265962.3:c.1504-8_1504-1del	XP_005266019.1:n.1504-8_1504-1del
XM_011534610.1:c.6010-8_6010-1del	XP_011532912.1:n.6010-8_6010-1del
XM_011534611.1:c.6010-8_6010-1del	XP_011532913.1:n.6010-8_6010-1del
XM_011534612.1:c.5590-8_5590-1del	XP_011532914.1:n.5590-8_5590-1del
XM_011534613.1:c.4954-8_4954-1del	XP_011532915.1:n.4954-8_4954-1del
XM_011534617.1:c.1744-8_1744-1del	XP_011532919.1:n.1744-8_1744-1del
NM_001365684.1:c.5203-8_5203-1del	NP_001352613.1:n.5203-8_5203-1del
XM_024446150.1:c.6010-8_6010-1del	XP_024301918.1:n.6010-8_6010-1del
XM_024446151.1:c.6010-8_6010-1del	XP_024301919.1:n.6010-8_6010-1del
XM_024446152.1:c.6010-8_6010-1del	XP_024301920.1:n.6010-8_6010-1del
XM_024446153.1:c.6010-8_6010-1del	XP_024301921.1:n.6010-8_6010-1del
XM_024446154.1:c.5590-8_5590-1del	XP_024301922.1:n.5590-8_5590-1del
XM_024446155.1:c.5203-8_5203-1del	XP_024301923.1:n.5203-8_5203-1del
XM_024446156.1:c.5203-8_5203-1del	XP_024301924.1:n.5203-8_5203-1del
XM_024446158.1:c.5203-8_5203-1del	XP_024301926.1:n.5203-8_5203-1del
XM_024446159.1:c.4954-8_4954-1del	XP_024301927.1:n.4954-8_4954-1del
XM_024446162.1:c.1744-8_1744-1del	XP_024301930.1:n.1744-8_1744-1del
XM_024446163.1:c.1504-8_1504-1del	XP_024301931.1:n.1504-8_1504-1del
NM_022455.5:c.6010-8_6010-1del MANE Select	NP_071900.2:n.6010-8_6010-1del
NM_172349.3:c.5203-8_5203-1del	NP_758859.1:n.5203-8_5203-1del