Canonical Allele Identifier: CA1603535239

Gene: NSD1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177293820_177293822delinsCTG , CM000667.2:g.177293820_177293822delinsCTG	GRCh38
NC_000005.9:g.176720821_176720823delinsCTG , CM000667.1:g.176720821_176720823delinsCTG	GRCh37
NC_000005.8:g.176653427_176653429delinsCTG	NCBI36
NG_009821.1:g.165742_165744delinsCTG , LRG_512:g.165742_165744delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508896.7:c.5591-12_5591-10delinsCTG	ENSP00000423372.3:n.5591-12_5591-10delinsCTG
ENST00000347982.9:c.5591-12_5591-10delinsCTG	ENSP00000343209.5:n.5591-12_5591-10delinsCTG
ENST00000354179.9:c.5591-12_5591-10delinsCTG	ENSP00000346111.5:n.5591-12_5591-10delinsCTG
ENST00000503056.6:c.1106-12_1106-10delinsCTG	ENSP00000424024.2:n.1106-12_1106-10delinsCTG
ENST00000508029.6:c.1106-12_1106-10delinsCTG	ENSP00000425120.2:n.1106-12_1106-10delinsCTG
ENST00000685206.1:n.6047-12_6047-10delinsCTG
ENST00000686385.1:n.880-12_880-10delinsCTG
ENST00000686993.1:c.5591-12_5591-10delinsCTG	ENSP00000510020.1:n.5591-12_5591-10delinsCTG
ENST00000687453.1:c.6155-12_6155-10delinsCTG	ENSP00000508426.1:n.6155-12_6155-10delinsCTG
ENST00000688613.1:n.5861-12_5861-10delinsCTG
ENST00000689345.1:c.5591-12_5591-10delinsCTG	ENSP00000509711.1:n.5591-12_5591-10delinsCTG
ENST00000439151.7:c.6464-12_6464-10delinsCTG MANE Select	ENSP00000395929.2:n.6464-12_6464-10delinsCTG
ENST00000347982.8:c.5657-12_5657-10delinsCTG	ENSP00000343209.4:n.5657-12_5657-10delinsCTG
ENST00000354179.8:c.5657-12_5657-10delinsCTG	ENSP00000346111.4:n.5657-12_5657-10delinsCTG
ENST00000439151.6:c.6464-12_6464-10delinsCTG	ENSP00000395929.2:n.6464-12_6464-10delinsCTG
NM_022455.4:c.6464-12_6464-10delinsCTG , LRG_512t1:c.6464-12_6464-10delinsCTG	NP_071900.2:n.6464-12_6464-10delinsCTG
NM_172349.2:c.5657-12_5657-10delinsCTG	NP_758859.1:n.5657-12_5657-10delinsCTG
XM_005265959.1:c.6464-12_6464-10delinsCTG	XP_005266016.1:n.6464-12_6464-10delinsCTG
XM_005265960.1:c.5657-12_5657-10delinsCTG	XP_005266017.1:n.5657-12_5657-10delinsCTG
XM_005265961.1:c.5657-12_5657-10delinsCTG	XP_005266018.1:n.5657-12_5657-10delinsCTG
XM_005265962.3:c.1958-12_1958-10delinsCTG	XP_005266019.1:n.1958-12_1958-10delinsCTG
XM_011534610.1:c.6464-12_6464-10delinsCTG	XP_011532912.1:n.6464-12_6464-10delinsCTG
XM_011534611.1:c.6464-12_6464-10delinsCTG	XP_011532913.1:n.6464-12_6464-10delinsCTG
XM_011534612.1:c.6044-12_6044-10delinsCTG	XP_011532914.1:n.6044-12_6044-10delinsCTG
XM_011534613.1:c.5408-12_5408-10delinsCTG	XP_011532915.1:n.5408-12_5408-10delinsCTG
XM_011534617.1:c.2198-12_2198-10delinsCTG	XP_011532919.1:n.2198-12_2198-10delinsCTG
NM_001365684.1:c.5657-12_5657-10delinsCTG	NP_001352613.1:n.5657-12_5657-10delinsCTG
XM_024446150.1:c.6464-12_6464-10delinsCTG	XP_024301918.1:n.6464-12_6464-10delinsCTG
XM_024446151.1:c.6464-12_6464-10delinsCTG	XP_024301919.1:n.6464-12_6464-10delinsCTG
XM_024446152.1:c.6464-12_6464-10delinsCTG	XP_024301920.1:n.6464-12_6464-10delinsCTG
XM_024446153.1:c.6464-12_6464-10delinsCTG	XP_024301921.1:n.6464-12_6464-10delinsCTG
XM_024446154.1:c.6044-12_6044-10delinsCTG	XP_024301922.1:n.6044-12_6044-10delinsCTG
XM_024446155.1:c.5657-12_5657-10delinsCTG	XP_024301923.1:n.5657-12_5657-10delinsCTG
XM_024446156.1:c.5657-12_5657-10delinsCTG	XP_024301924.1:n.5657-12_5657-10delinsCTG
XM_024446158.1:c.5657-12_5657-10delinsCTG	XP_024301926.1:n.5657-12_5657-10delinsCTG
XM_024446159.1:c.5408-12_5408-10delinsCTG	XP_024301927.1:n.5408-12_5408-10delinsCTG
XM_024446162.1:c.2198-12_2198-10delinsCTG	XP_024301930.1:n.2198-12_2198-10delinsCTG
XM_024446163.1:c.1958-12_1958-10delinsCTG	XP_024301931.1:n.1958-12_1958-10delinsCTG
NM_022455.5:c.6464-12_6464-10delinsCTG MANE Select	NP_071900.2:n.6464-12_6464-10delinsCTG
NM_172349.3:c.5657-12_5657-10delinsCTG	NP_758859.1:n.5657-12_5657-10delinsCTG