Canonical Allele Identifier: CA2788377812
Gene: MYPN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68166547_68166548insC , CM000672.2:g.68166547_68166548insC GRCh38
NC_000010.10:g.69926304_69926305insC , CM000672.1:g.69926304_69926305insC GRCh37
NC_000010.9:g.69596310_69596311insC NCBI36
NG_032118.1:g.65431_65432insC , LRG_410:g.65431_65432insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000354393.7:c.1029_1030insC ENSP00000346369.2:p.Thr344HisfsTer?
ENST00000373675.4:c.1854_1855insC ENSP00000362779.4:p.Thr619HisfsTer?
ENST00000540630.6:c.1908_1909insC ENSP00000441668.3:p.Thr637HisfsTer?
ENST00000613327.5:c.1854_1855insC ENSP00000480757.2:p.Thr619HisfsTer?
ENST00000687572.1:c.732_733insC ENSP00000510427.1:p.Thr245HisfsTer?
ENST00000688812.1:c.1830_1831insC ENSP00000510658.1:p.Thr611HisfsTer?
ENST00000690544.1:c.*1125_*1126insC ENSP00000508989.1:n.*1125_*1126insC
ENST00000358913.10:c.1854_1855insC MANE Select ENSP00000351790.5:p.Thr619HisfsTer?
ENST00000354393.6:c.1029_1030insC ENSP00000346369.2:p.Thr344HisfsTer?
ENST00000358913.9:c.1854_1855insC ENSP00000351790.5:p.Thr619HisfsTer?
ENST00000540630.5:c.1854_1855insC ENSP00000441668.2:p.Thr619HisfsTer?
ENST00000613327.4:c.972_973insC ENSP00000480757.1:p.Thr325HisfsTer?
NM_001256267.1:c.1854_1855insC NP_001243196.1:p.Thr619HisfsTer?
NM_001256268.1:c.972_973insC NP_001243197.1:p.Thr325HisfsTer?
NM_032578.3:c.1854_1855insC , LRG_410t1:c.1854_1855insC NP_115967.2:p.Thr619HisfsTer?
NR_045662.3:n.1281_1282insC
NR_045663.3:n.2122_2123insC
XM_006718043.2:c.1908_1909insC XP_006718106.1:p.Thr637HisfsTer?
XM_011540292.1:c.1884_1885insC XP_011538594.1:p.Thr629HisfsTer?
XM_017016833.1:c.1932_1933insC XP_016872322.1:p.Thr645HisfsTer?
XM_017016834.2:c.1854_1855insC XP_016872323.1:p.Thr619HisfsTer?
XM_024448236.1:c.732_733insC XP_024304004.1:p.Thr245HisfsTer?
NR_045662.4:n.1391_1392insC
NR_045663.4:n.2067_2068insC
NM_001256267.2:c.1854_1855insC NP_001243196.1:p.Thr619HisfsTer?
NM_001256268.2:c.972_973insC NP_001243197.1:p.Thr325HisfsTer?
NM_032578.4:c.1854_1855insC MANE Select NP_115967.2:p.Thr619HisfsTer?