Canonical Allele Identifier: CA2538050649
Gene: NSD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.177211866_177211867insGTATCAT , CM000667.2:g.177211866_177211867insGTATCAT GRCh38
NC_000005.9:g.176638867_176638868insGTATCAT , CM000667.1:g.176638867_176638868insGTATCAT GRCh37
NC_000005.8:g.176571473_176571474insGTATCAT NCBI36
NG_009821.1:g.83788_83789insGTATCAT , LRG_512:g.83788_83789insGTATCAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000508896.7:c.2594_2595insGTATCAT ENSP00000423372.3:p.Lys866TyrfsTer3
ENST00000347982.9:c.2594_2595insGTATCAT ENSP00000343209.5:p.Lys866TyrfsTer3
ENST00000354179.9:c.2594_2595insGTATCAT ENSP00000346111.5:p.Lys866TyrfsTer3
ENST00000510954.6:n.612+7574_612+7575insGTATCAT
ENST00000685206.1:n.3050_3051insGTATCAT
ENST00000686993.1:c.2594_2595insGTATCAT ENSP00000510020.1:p.Lys866TyrfsTer3
ENST00000687453.1:c.3158_3159insGTATCAT ENSP00000508426.1:p.Lys1054TyrfsTer3
ENST00000688613.1:n.2864_2865insGTATCAT
ENST00000689326.1:c.3467_3468insGTATCAT ENSP00000509594.1:p.Lys1157TyrfsTer3
ENST00000689345.1:c.2594_2595insGTATCAT ENSP00000509711.1:p.Lys866TyrfsTer3
ENST00000689549.1:n.3614_3615insGTATCAT
ENST00000439151.7:c.3467_3468insGTATCAT MANE Select ENSP00000395929.2:p.Lys1157TyrfsTer3
ENST00000347982.8:c.2660_2661insGTATCAT ENSP00000343209.4:p.Lys888TyrfsTer3
ENST00000354179.8:c.2660_2661insGTATCAT ENSP00000346111.4:p.Lys888TyrfsTer3
ENST00000439151.6:c.3467_3468insGTATCAT ENSP00000395929.2:p.Lys1157TyrfsTer3
NM_022455.4:c.3467_3468insGTATCAT , LRG_512t1:c.3467_3468insGTATCAT NP_071900.2:p.Lys1157TyrfsTer3
NM_172349.2:c.2660_2661insGTATCAT NP_758859.1:p.Lys888TyrfsTer3
XM_005265959.1:c.3467_3468insGTATCAT XP_005266016.1:p.Lys1157TyrfsTer3
XM_005265960.1:c.2660_2661insGTATCAT XP_005266017.1:p.Lys888TyrfsTer3
XM_005265961.1:c.2660_2661insGTATCAT XP_005266018.1:p.Lys888TyrfsTer3
XM_011534610.1:c.3467_3468insGTATCAT XP_011532912.1:p.Lys1157TyrfsTer3
XM_011534611.1:c.3467_3468insGTATCAT XP_011532913.1:p.Lys1157TyrfsTer3
XM_011534612.1:c.3047_3048insGTATCAT XP_011532914.1:p.Lys1017TyrfsTer3
XM_011534613.1:c.2411_2412insGTATCAT XP_011532915.1:p.Lys805TyrfsTer3
XM_011534614.1:c.3467_3468insGTATCAT XP_011532916.1:p.Lys1157TyrfsTer3
XM_011534615.1:c.3467_3468insGTATCAT XP_011532917.1:p.Lys1157TyrfsTer3
XM_011534616.1:c.3467_3468insGTATCAT XP_011532918.1:p.Lys1157TyrfsTer3
NM_001365684.1:c.2660_2661insGTATCAT NP_001352613.1:p.Lys888TyrfsTer3
XM_024446150.1:c.3467_3468insGTATCAT XP_024301918.1:p.Lys1157TyrfsTer3
XM_024446151.1:c.3467_3468insGTATCAT XP_024301919.1:p.Lys1157TyrfsTer3
XM_024446152.1:c.3467_3468insGTATCAT XP_024301920.1:p.Lys1157TyrfsTer3
XM_024446153.1:c.3467_3468insGTATCAT XP_024301921.1:p.Lys1157TyrfsTer3
XM_024446154.1:c.3047_3048insGTATCAT XP_024301922.1:p.Lys1017TyrfsTer3
XM_024446155.1:c.2660_2661insGTATCAT XP_024301923.1:p.Lys888TyrfsTer3
XM_024446156.1:c.2660_2661insGTATCAT XP_024301924.1:p.Lys888TyrfsTer3
XM_024446158.1:c.2660_2661insGTATCAT XP_024301926.1:p.Lys888TyrfsTer3
XM_024446159.1:c.2411_2412insGTATCAT XP_024301927.1:p.Lys805TyrfsTer3
XM_024446160.1:c.3467_3468insGTATCAT XP_024301928.1:p.Lys1157TyrfsTer3
XM_024446161.1:c.3467_3468insGTATCAT XP_024301929.1:p.Lys1157TyrfsTer3
XM_024446162.1:c.-529_-528insGTATCAT XP_024301930.1:n.-529_-528insGTATCAT
NM_022455.5:c.3467_3468insGTATCAT MANE Select NP_071900.2:p.Lys1157TyrfsTer3
NM_172349.3:c.2660_2661insGTATCAT NP_758859.1:p.Lys888TyrfsTer3