Canonical Allele Identifier: CA1917232498
Gene: MYPN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68210537_68210538delinsAC , CM000672.2:g.68210537_68210538delinsAC GRCh38
NC_000010.10:g.69970294_69970295delinsAC , CM000672.1:g.69970294_69970295delinsAC GRCh37
NC_000010.9:g.69640300_69640301delinsAC NCBI36
NG_032118.1:g.109421_109422delinsAC , LRG_410:g.109421_109422delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000354393.7:c.*82_*83delinsAC ENSP00000346369.2:n.*82_*83delinsAC
ENST00000540630.6:c.*82_*83delinsAC ENSP00000441668.3:n.*82_*83delinsAC
ENST00000613327.5:c.*82_*83delinsAC ENSP00000480757.2:n.*82_*83delinsAC
ENST00000688812.1:c.*1308_*1309delinsAC ENSP00000510658.1:n.*1308_*1309delinsAC
ENST00000690544.1:c.*3316_*3317delinsAC ENSP00000508989.1:n.*3316_*3317delinsAC
ENST00000358913.10:c.*82_*83delinsAC MANE Select ENSP00000351790.5:n.*82_*83delinsAC
ENST00000354393.6:c.*82_*83delinsAC ENSP00000346369.2:n.*82_*83delinsAC
ENST00000358913.9:c.*82_*83delinsAC ENSP00000351790.5:n.*82_*83delinsAC
ENST00000540630.5:c.*82_*83delinsAC ENSP00000441668.2:n.*82_*83delinsAC
ENST00000613327.4:c.*82_*83delinsAC ENSP00000480757.1:n.*82_*83delinsAC
NM_001256267.1:c.*82_*83delinsAC NP_001243196.1:n.*82_*83delinsAC
NM_001256268.1:c.*82_*83delinsAC NP_001243197.1:n.*82_*83delinsAC
NM_032578.3:c.*82_*83delinsAC , LRG_410t1:c.*82_*83delinsAC NP_115967.2:n.*82_*83delinsAC
NR_045662.3:n.3472_3473delinsAC
NR_045663.3:n.4174_4175delinsAC
XM_006718043.2:c.*82_*83delinsAC XP_006718106.1:n.*82_*83delinsAC
XM_011540292.1:c.*82_*83delinsAC XP_011538594.1:n.*82_*83delinsAC
XR_946029.1:n.1574+4750_1574+4751delinsGT
XM_017016833.1:c.*82_*83delinsAC XP_016872322.1:n.*82_*83delinsAC
XM_017016834.2:c.*82_*83delinsAC XP_016872323.1:n.*82_*83delinsAC
XM_024448236.1:c.*82_*83delinsAC XP_024304004.1:n.*82_*83delinsAC
NR_045662.4:n.3582_3583delinsAC
NR_045663.4:n.4119_4120delinsAC
NM_001256267.2:c.*82_*83delinsAC NP_001243196.1:n.*82_*83delinsAC
NM_001256268.2:c.*82_*83delinsAC NP_001243197.1:n.*82_*83delinsAC
NM_032578.4:c.*82_*83delinsAC MANE Select NP_115967.2:n.*82_*83delinsAC