Canonical Allele Identifier: CA2609374251
Gene: MYPN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68210581_68210582del , CM000672.2:g.68210581_68210582del GRCh38
NC_000010.10:g.69970338_69970339del , CM000672.1:g.69970338_69970339del GRCh37
NC_000010.9:g.69640344_69640345del NCBI36
NG_032118.1:g.109465_109466del , LRG_410:g.109465_109466del

Transcript Alleles

HGVS Amino-acid Change
ENST00000354393.7:c.*126_*127del ENSP00000346369.2:n.*126_*127del
ENST00000540630.6:c.*126_*127del ENSP00000441668.3:n.*126_*127del
ENST00000613327.5:c.*126_*127del ENSP00000480757.2:n.*126_*127del
ENST00000688812.1:c.*1352_*1353del ENSP00000510658.1:n.*1352_*1353del
ENST00000690544.1:c.*3360_*3361del ENSP00000508989.1:n.*3360_*3361del
ENST00000358913.10:c.*126_*127del MANE Select ENSP00000351790.5:n.*126_*127del
ENST00000354393.6:c.*126_*127del ENSP00000346369.2:n.*126_*127del
ENST00000358913.9:c.*126_*127del ENSP00000351790.5:n.*126_*127del
ENST00000540630.5:c.*126_*127del ENSP00000441668.2:n.*126_*127del
ENST00000613327.4:c.*126_*127del ENSP00000480757.1:n.*126_*127del
NM_001256267.1:c.*126_*127del NP_001243196.1:n.*126_*127del
NM_001256268.1:c.*126_*127del NP_001243197.1:n.*126_*127del
NM_032578.3:c.*126_*127del , LRG_410t1:c.*126_*127del NP_115967.2:n.*126_*127del
NR_045662.3:n.3516_3517del
NR_045663.3:n.4218_4219del
XM_006718043.2:c.*126_*127del XP_006718106.1:n.*126_*127del
XM_011540292.1:c.*126_*127del XP_011538594.1:n.*126_*127del
XR_946029.1:n.1574+4708_1574+4709del
XM_017016833.1:c.*126_*127del XP_016872322.1:n.*126_*127del
XM_017016834.2:c.*126_*127del XP_016872323.1:n.*126_*127del
XM_024448236.1:c.*126_*127del XP_024304004.1:n.*126_*127del
NR_045662.4:n.3626_3627del
NR_045663.4:n.4163_4164del
NM_001256267.2:c.*126_*127del NP_001243196.1:n.*126_*127del
NM_001256268.2:c.*126_*127del NP_001243197.1:n.*126_*127del
NM_032578.4:c.*126_*127del MANE Select NP_115967.2:n.*126_*127del