Canonical Allele Identifier: CA1603533397
Gene: NSD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177264234_177264235delinsAT , CM000667.2:g.177264234_177264235delinsAT GRCh38
NC_000005.9:g.176691235_176691236delinsAT , CM000667.1:g.176691235_176691236delinsAT GRCh37
NC_000005.8:g.176623841_176623842delinsAT NCBI36
NG_009821.1:g.136156_136157delinsAT , LRG_512:g.136156_136157delinsAT

Transcript Alleles

HGVS Amino-acid change
ENST00000508896.7:c.4274-3328_4274-3327delinsAT ENSP00000423372.3:n.4274-3328_4274-3327de...
ENST00000347982.9:c.4274-3328_4274-3327delinsAT ENSP00000343209.5:n.4274-3328_4274-3327de...
ENST00000354179.9:c.4274-3328_4274-3327delinsAT ENSP00000346111.5:n.4274-3328_4274-3327de...
ENST00000685206.1:n.4730-3328_4730-3327delinsAT
ENST00000686993.1:c.4274-3328_4274-3327delinsAT ENSP00000510020.1:n.4274-3328_4274-3327de...
ENST00000687453.1:c.4838-3328_4838-3327delinsAT ENSP00000508426.1:n.4838-3328_4838-3327de...
ENST00000688613.1:n.4544-3328_4544-3327delinsAT
ENST00000689345.1:c.4274-3328_4274-3327delinsAT ENSP00000509711.1:n.4274-3328_4274-3327de...
ENST00000689549.1:n.5294-3328_5294-3327delinsAT
ENST00000439151.7:c.5147-3328_5147-3327delinsAT MANE Select ENSP00000395929.2:n.5147-3328_5147-3327de...
ENST00000347982.8:c.4340-3328_4340-3327delinsAT ENSP00000343209.4:n.4340-3328_4340-3327de...
ENST00000354179.8:c.4340-3328_4340-3327delinsAT ENSP00000346111.4:n.4340-3328_4340-3327de...
ENST00000439151.6:c.5147-3328_5147-3327delinsAT ENSP00000395929.2:n.5147-3328_5147-3327de...
NM_022455.4:c.5147-3328_5147-3327delinsAT , LRG_512t1:c.5147-3328_5147-3327delinsAT NP_071900.2:n.5147-3328_5147-3327delinsAT...
NM_172349.2:c.4340-3328_4340-3327delinsAT NP_758859.1:n.4340-3328_4340-3327delinsAT...
XM_005265959.1:c.5147-3328_5147-3327delinsAT XP_005266016.1:n.5147-3328_5147-3327delin...
XM_005265960.1:c.4340-3328_4340-3327delinsAT XP_005266017.1:n.4340-3328_4340-3327delin...
XM_005265961.1:c.4340-3328_4340-3327delinsAT XP_005266018.1:n.4340-3328_4340-3327delin...
XM_005265962.3:c.641-3328_641-3327delinsAT XP_005266019.1:n.641-3328_641-3327delinsA...
XM_011534610.1:c.5147-3328_5147-3327delinsAT XP_011532912.1:n.5147-3328_5147-3327delin...
XM_011534611.1:c.5147-3328_5147-3327delinsAT XP_011532913.1:n.5147-3328_5147-3327delin...
XM_011534612.1:c.4727-3328_4727-3327delinsAT XP_011532914.1:n.4727-3328_4727-3327delin...
XM_011534613.1:c.4091-3328_4091-3327delinsAT XP_011532915.1:n.4091-3328_4091-3327delin...
XM_011534617.1:c.881-3328_881-3327delinsAT XP_011532919.1:n.881-3328_881-3327delinsA...
NM_001365684.1:c.4340-3328_4340-3327delinsAT NP_001352613.1:n.4340-3328_4340-3327delin...
XM_024446150.1:c.5147-3328_5147-3327delinsAT XP_024301918.1:n.5147-3328_5147-3327delin...
XM_024446151.1:c.5147-3328_5147-3327delinsAT XP_024301919.1:n.5147-3328_5147-3327delin...
XM_024446152.1:c.5147-3328_5147-3327delinsAT XP_024301920.1:n.5147-3328_5147-3327delin...
XM_024446153.1:c.5147-3328_5147-3327delinsAT XP_024301921.1:n.5147-3328_5147-3327delin...
XM_024446154.1:c.4727-3328_4727-3327delinsAT XP_024301922.1:n.4727-3328_4727-3327delin...
XM_024446155.1:c.4340-3328_4340-3327delinsAT XP_024301923.1:n.4340-3328_4340-3327delin...
XM_024446156.1:c.4340-3328_4340-3327delinsAT XP_024301924.1:n.4340-3328_4340-3327delin...
XM_024446158.1:c.4340-3328_4340-3327delinsAT XP_024301926.1:n.4340-3328_4340-3327delin...
XM_024446159.1:c.4091-3328_4091-3327delinsAT XP_024301927.1:n.4091-3328_4091-3327delin...
XM_024446162.1:c.881-3328_881-3327delinsAT XP_024301930.1:n.881-3328_881-3327delinsA...
XM_024446163.1:c.641-3328_641-3327delinsAT XP_024301931.1:n.641-3328_641-3327delinsA...
NM_022455.5:c.5147-3328_5147-3327delinsAT MANE Select NP_071900.2:n.5147-3328_5147-3327delinsAT...
NM_172349.3:c.4340-3328_4340-3327delinsAT NP_758859.1:n.4340-3328_4340-3327delinsAT...