Canonical Allele Identifier: CA1603535682

Gene: NSD1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177294051_177294052delinsTG , CM000667.2:g.177294051_177294052delinsTG	GRCh38
NC_000005.9:g.176721052_176721053delinsTG , CM000667.1:g.176721052_176721053delinsTG	GRCh37
NC_000005.8:g.176653658_176653659delinsTG	NCBI36
NG_009821.1:g.165973_165974delinsTG , LRG_512:g.165973_165974delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508896.7:c.5810_5811delinsTG	ENSP00000423372.3:p.Leu1937=
ENST00000347982.9:c.5810_5811delinsTG	ENSP00000343209.5:p.Leu1937=
ENST00000354179.9:c.5810_5811delinsTG	ENSP00000346111.5:p.Leu1937=
ENST00000503056.6:c.1325_1326delinsTG	ENSP00000424024.2:p.Leu442=
ENST00000508029.6:c.1325_1326delinsTG	ENSP00000425120.2:p.Leu442=
ENST00000685206.1:n.6266_6267delinsTG
ENST00000686385.1:n.1099_1100delinsTG
ENST00000686993.1:c.5810_5811delinsTG	ENSP00000510020.1:p.Leu1937=
ENST00000687453.1:c.6374_6375delinsTG	ENSP00000508426.1:p.Leu2125=
ENST00000688613.1:n.6080_6081delinsTG
ENST00000689345.1:c.5810_5811delinsTG	ENSP00000509711.1:p.Leu1937=
ENST00000439151.7:c.6683_6684delinsTG MANE Select	ENSP00000395929.2:p.Leu2228=
ENST00000347982.8:c.5876_5877delinsTG	ENSP00000343209.4:p.Leu1959=
ENST00000354179.8:c.5876_5877delinsTG	ENSP00000346111.4:p.Leu1959=
ENST00000439151.6:c.6683_6684delinsTG	ENSP00000395929.2:p.Leu2228=
NM_022455.4:c.6683_6684delinsTG , LRG_512t1:c.6683_6684delinsTG	NP_071900.2:p.Leu2228=
NM_172349.2:c.5876_5877delinsTG	NP_758859.1:p.Leu1959=
XM_005265959.1:c.6683_6684delinsTG	XP_005266016.1:p.Leu2228=
XM_005265960.1:c.5876_5877delinsTG	XP_005266017.1:p.Leu1959=
XM_005265961.1:c.5876_5877delinsTG	XP_005266018.1:p.Leu1959=
XM_005265962.3:c.2177_2178delinsTG	XP_005266019.1:p.Leu726=
XM_011534610.1:c.6683_6684delinsTG	XP_011532912.1:p.Leu2228=
XM_011534611.1:c.6683_6684delinsTG	XP_011532913.1:p.Leu2228=
XM_011534612.1:c.6263_6264delinsTG	XP_011532914.1:p.Leu2088=
XM_011534613.1:c.5627_5628delinsTG	XP_011532915.1:p.Leu1876=
XM_011534617.1:c.2417_2418delinsTG	XP_011532919.1:p.Leu806=
NM_001365684.1:c.5876_5877delinsTG	NP_001352613.1:p.Leu1959=
XM_024446150.1:c.6683_6684delinsTG	XP_024301918.1:p.Leu2228=
XM_024446151.1:c.6683_6684delinsTG	XP_024301919.1:p.Leu2228=
XM_024446152.1:c.6683_6684delinsTG	XP_024301920.1:p.Leu2228=
XM_024446153.1:c.6683_6684delinsTG	XP_024301921.1:p.Leu2228=
XM_024446154.1:c.6263_6264delinsTG	XP_024301922.1:p.Leu2088=
XM_024446155.1:c.5876_5877delinsTG	XP_024301923.1:p.Leu1959=
XM_024446156.1:c.5876_5877delinsTG	XP_024301924.1:p.Leu1959=
XM_024446158.1:c.5876_5877delinsTG	XP_024301926.1:p.Leu1959=
XM_024446159.1:c.5627_5628delinsTG	XP_024301927.1:p.Leu1876=
XM_024446162.1:c.2417_2418delinsTG	XP_024301930.1:p.Leu806=
XM_024446163.1:c.2177_2178delinsTG	XP_024301931.1:p.Leu726=
NM_022455.5:c.6683_6684delinsTG MANE Select	NP_071900.2:p.Leu2228=
NM_172349.3:c.5876_5877delinsTG	NP_758859.1:p.Leu1959=