Canonical Allele Identifier: CA1603552039

Gene: NSD1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177282514_177282515delinsGC , CM000667.2:g.177282514_177282515delinsGC	GRCh38
NC_000005.9:g.176709515_176709516delinsGC , CM000667.1:g.176709515_176709516delinsGC	GRCh37
NC_000005.8:g.176642121_176642122delinsGC	NCBI36
NG_009821.1:g.154436_154437delinsGC , LRG_512:g.154436_154437delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000508896.7:c.5069_5070delinsGC	ENSP00000423372.3:p.Cys1690=
ENST00000347982.9:c.5069_5070delinsGC	ENSP00000343209.5:p.Cys1690=
ENST00000354179.9:c.5069_5070delinsGC	ENSP00000346111.5:p.Cys1690=
ENST00000503056.6:c.584_585delinsGC	ENSP00000424024.2:p.Cys195=
ENST00000508029.6:c.584_585delinsGC	ENSP00000425120.2:p.Cys195=
ENST00000685206.1:n.5525_5526delinsGC
ENST00000686993.1:c.5069_5070delinsGC	ENSP00000510020.1:p.Cys1690=
ENST00000687453.1:c.5633_5634delinsGC	ENSP00000508426.1:p.Cys1878=
ENST00000688613.1:n.5339_5340delinsGC
ENST00000689345.1:c.5069_5070delinsGC	ENSP00000509711.1:p.Cys1690=
ENST00000689549.1:n.6089_6090delinsGC
ENST00000692024.1:n.4491_4492delinsGC
ENST00000439151.7:c.5942_5943delinsGC MANE Select	ENSP00000395929.2:p.Cys1981=
ENST00000347982.8:c.5135_5136delinsGC	ENSP00000343209.4:p.Cys1712=
ENST00000354179.8:c.5135_5136delinsGC	ENSP00000346111.4:p.Cys1712=
ENST00000439151.6:c.5942_5943delinsGC	ENSP00000395929.2:p.Cys1981=
NM_022455.4:c.5942_5943delinsGC , LRG_512t1:c.5942_5943delinsGC	NP_071900.2:p.Cys1981=
NM_172349.2:c.5135_5136delinsGC	NP_758859.1:p.Cys1712=
XM_005265959.1:c.5942_5943delinsGC	XP_005266016.1:p.Cys1981=
XM_005265960.1:c.5135_5136delinsGC	XP_005266017.1:p.Cys1712=
XM_005265961.1:c.5135_5136delinsGC	XP_005266018.1:p.Cys1712=
XM_005265962.3:c.1436_1437delinsGC	XP_005266019.1:p.Cys479=
XM_011534610.1:c.5942_5943delinsGC	XP_011532912.1:p.Cys1981=
XM_011534611.1:c.5942_5943delinsGC	XP_011532913.1:p.Cys1981=
XM_011534612.1:c.5522_5523delinsGC	XP_011532914.1:p.Cys1841=
XM_011534613.1:c.4886_4887delinsGC	XP_011532915.1:p.Cys1629=
XM_011534617.1:c.1676_1677delinsGC	XP_011532919.1:p.Cys559=
NM_001365684.1:c.5135_5136delinsGC	NP_001352613.1:p.Cys1712=
XM_024446150.1:c.5942_5943delinsGC	XP_024301918.1:p.Cys1981=
XM_024446151.1:c.5942_5943delinsGC	XP_024301919.1:p.Cys1981=
XM_024446152.1:c.5942_5943delinsGC	XP_024301920.1:p.Cys1981=
XM_024446153.1:c.5942_5943delinsGC	XP_024301921.1:p.Cys1981=
XM_024446154.1:c.5522_5523delinsGC	XP_024301922.1:p.Cys1841=
XM_024446155.1:c.5135_5136delinsGC	XP_024301923.1:p.Cys1712=
XM_024446156.1:c.5135_5136delinsGC	XP_024301924.1:p.Cys1712=
XM_024446158.1:c.5135_5136delinsGC	XP_024301926.1:p.Cys1712=
XM_024446159.1:c.4886_4887delinsGC	XP_024301927.1:p.Cys1629=
XM_024446162.1:c.1676_1677delinsGC	XP_024301930.1:p.Cys559=
XM_024446163.1:c.1436_1437delinsGC	XP_024301931.1:p.Cys479=
NM_022455.5:c.5942_5943delinsGC MANE Select	NP_071900.2:p.Cys1981=
NM_172349.3:c.5135_5136delinsGC	NP_758859.1:p.Cys1712=