Canonical Allele Identifier: CA1917215573
Gene: MYPN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68165712C= , CM000672.2:g.68165712C= GRCh38
NC_000010.10:g.69925469C= , CM000672.1:g.69925469C= GRCh37
NC_000010.9:g.69595475C= NCBI36
NG_032118.1:g.64596C= , LRG_410:g.64596C=

Transcript Alleles

HGVS Amino-acid change
ENST00000354393.7:c.669C= ENSP00000346369.2:p.Cys223=
ENST00000373675.4:c.1494C= ENSP00000362779.4:p.Cys498=
ENST00000540630.6:c.1548C= ENSP00000441668.3:p.Cys516=
ENST00000613327.5:c.1494C= ENSP00000480757.2:p.Cys498=
ENST00000687572.1:c.372C= ENSP00000510427.1:p.Cys124=
ENST00000687705.1:c.*1743C= ENSP00000509639.1:n.*1743C=
ENST00000688812.1:c.1470C= ENSP00000510658.1:p.Cys490=
ENST00000689002.1:n.546C=
ENST00000690544.1:c.*765C= ENSP00000508989.1:n.*765C=
ENST00000358913.10:c.1494C= MANE Select ENSP00000351790.5:p.Cys498=
ENST00000354393.6:c.669C= ENSP00000346369.2:p.Cys223=
ENST00000358913.9:c.1494C= ENSP00000351790.5:p.Cys498=
ENST00000540630.5:c.1494C= ENSP00000441668.2:p.Cys498=
ENST00000613327.4:c.612C= ENSP00000480757.1:p.Cys204=
NM_001256267.1:c.1494C= NP_001243196.1:p.Cys498=
NM_001256268.1:c.612C= NP_001243197.1:p.Cys204=
NM_032578.3:c.1494C= , LRG_410t1:c.1494C= NP_115967.2:p.Cys498=
NR_045662.3:n.921C=
NR_045663.3:n.1762C=
XM_006718043.2:c.1548C= XP_006718106.1:p.Cys516=
XM_011540292.1:c.1524C= XP_011538594.1:p.Cys508=
XM_017016833.1:c.1572C= XP_016872322.1:p.Cys524=
XM_017016834.2:c.1494C= XP_016872323.1:p.Cys498=
XM_024448236.1:c.372C= XP_024304004.1:p.Cys124=
NR_045662.4:n.1031C=
NR_045663.4:n.1707C=
NM_001256267.2:c.1494C= NP_001243196.1:p.Cys498=
NM_001256268.2:c.612C= NP_001243197.1:p.Cys204=
NM_032578.4:c.1494C= MANE Select NP_115967.2:p.Cys498=