Canonical Allele Identifier: CA2609373570
Gene: MYPN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68199481_68199504del , CM000672.2:g.68199481_68199504del GRCh38
NC_000010.10:g.69959238_69959261del , CM000672.1:g.69959238_69959261del GRCh37
NC_000010.9:g.69629244_69629267del NCBI36
NG_032118.1:g.98365_98388del , LRG_410:g.98365_98388del

Transcript Alleles

HGVS Amino-acid Change
ENST00000354393.7:c.2574_2597del ENSP00000346369.2:p.Asp859_Ala866del
ENST00000540630.6:c.3453_3476del ENSP00000441668.3:p.Asp1152_Ala1159del
ENST00000613327.5:c.3399_3422del ENSP00000480757.2:p.Asp1134_Ala1141del
ENST00000688812.1:c.*662_*685del ENSP00000510658.1:n.*662_*685del
ENST00000690544.1:c.*2670_*2693del ENSP00000508989.1:n.*2670_*2693del
ENST00000358913.10:c.3399_3422del MANE Select ENSP00000351790.5:p.Asp1134_Ala1141del
ENST00000354393.6:c.2574_2597del ENSP00000346369.2:p.Asp859_Ala866del
ENST00000358913.9:c.3399_3422del ENSP00000351790.5:p.Asp1134_Ala1141del
ENST00000540630.5:c.3399_3422del ENSP00000441668.2:p.Asp1134_Ala1141del
ENST00000613327.4:c.2517_2540del ENSP00000480757.1:p.Asp840_Ala847del
NM_001256267.1:c.3399_3422del NP_001243196.1:p.Asp1134_Ala1141del
NM_001256268.1:c.2517_2540del NP_001243197.1:p.Asp840_Ala847del
NM_032578.3:c.3399_3422del , LRG_410t1:c.3399_3422del NP_115967.2:p.Asp1134_Ala1141del
NR_045662.3:n.2826_2849del
NR_045663.3:n.3528_3551del
XM_006718043.2:c.3453_3476del XP_006718106.1:p.Asp1152_Ala1159del
XM_011540292.1:c.3429_3452del XP_011538594.1:p.Asp1144_Ala1151del
XR_946029.1:n.1804-229_1804-206del
XM_017016833.1:c.3477_3500del XP_016872322.1:p.Asp1160_Ala1167del
XM_017016834.2:c.3399_3422del XP_016872323.1:p.Asp1134_Ala1141del
XM_024448236.1:c.2277_2300del XP_024304004.1:p.Asp760_Ala767del
NR_045662.4:n.2936_2959del
NR_045663.4:n.3473_3496del
NM_001256267.2:c.3399_3422del NP_001243196.1:p.Asp1134_Ala1141del
NM_001256268.2:c.2517_2540del NP_001243197.1:p.Asp840_Ala847del
NM_032578.4:c.3399_3422del MANE Select NP_115967.2:p.Asp1134_Ala1141del