Canonical Allele Identifier: CA667794318
Gene: MYPN HGNC NCBI

Linked Data

dbSNP Id: rs1204645657

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68166266dup , CM000672.2:g.68166266dup GRCh38
NC_000010.10:g.69926023dup , CM000672.1:g.69926023dup GRCh37
NC_000010.9:g.69596029dup NCBI36
NG_032118.1:g.65150dup , LRG_410:g.65150dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000354393.7:c.776-28dup ENSP00000346369.2:n.776-28dup
ENST00000373675.4:c.1601-28dup ENSP00000362779.4:n.1601-28dup
ENST00000540630.6:c.1655-28dup ENSP00000441668.3:n.1655-28dup
ENST00000613327.5:c.1601-28dup ENSP00000480757.2:n.1601-28dup
ENST00000687572.1:c.479-28dup ENSP00000510427.1:n.479-28dup
ENST00000687705.1:c.*1850-28dup ENSP00000509639.1:n.*1850-28dup
ENST00000688812.1:c.1577-28dup ENSP00000510658.1:n.1577-28dup
ENST00000689002.1:n.653-28dup
ENST00000690544.1:c.*872-28dup ENSP00000508989.1:n.*872-28dup
ENST00000358913.10:c.1601-28dup MANE Select ENSP00000351790.5:n.1601-28dup
ENST00000354393.6:c.776-28dup ENSP00000346369.2:n.776-28dup
ENST00000358913.9:c.1601-28dup ENSP00000351790.5:n.1601-28dup
ENST00000540630.5:c.1601-28dup ENSP00000441668.2:n.1601-28dup
ENST00000613327.4:c.719-28dup ENSP00000480757.1:n.719-28dup
NM_001256267.1:c.1601-28dup NP_001243196.1:n.1601-28dup
NM_001256268.1:c.719-28dup NP_001243197.1:n.719-28dup
NM_032578.3:c.1601-28dup , LRG_410t1:c.1601-28dup NP_115967.2:n.1601-28dup
NR_045662.3:n.1028-28dup
NR_045663.3:n.1869-28dup
XM_006718043.2:c.1655-28dup XP_006718106.1:n.1655-28dup
XM_011540292.1:c.1631-28dup XP_011538594.1:n.1631-28dup
XM_017016833.1:c.1679-28dup XP_016872322.1:n.1679-28dup
XM_017016834.2:c.1601-28dup XP_016872323.1:n.1601-28dup
XM_024448236.1:c.479-28dup XP_024304004.1:n.479-28dup
NR_045662.4:n.1138-28dup
NR_045663.4:n.1814-28dup
NM_001256267.2:c.1601-28dup NP_001243196.1:n.1601-28dup
NM_001256268.2:c.719-28dup NP_001243197.1:n.719-28dup
NM_032578.4:c.1601-28dup MANE Select NP_115967.2:n.1601-28dup