Canonical Allele Identifier: CA1917192600
Gene: MYPN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68122194A= , CM000672.2:g.68122194A= GRCh38
NC_000010.10:g.69881951A= , CM000672.1:g.69881951A= GRCh37
NC_000010.9:g.69551957A= NCBI36
NG_032118.1:g.21078A= , LRG_410:g.21078A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000354393.7:c.77+15393A= ENSP00000346369.2:n.77+15393A=
ENST00000373675.4:c.756A= ENSP00000362779.4:p.Pro252=
ENST00000540630.6:c.756A= ENSP00000441668.3:p.Pro252=
ENST00000613327.5:c.756A= ENSP00000480757.2:p.Pro252=
ENST00000685006.1:c.828A= ENSP00000510318.1:p.Pro276=
ENST00000685060.1:n.993A=
ENST00000685154.1:c.756A= ENSP00000509251.1:p.Pro252=
ENST00000685627.1:c.*767A= ENSP00000508637.1:n.*767A=
ENST00000686289.1:n.113+16011A=
ENST00000687572.1:c.-221+16011A= ENSP00000510427.1:n.-221+16011A=
ENST00000687705.1:c.*1005A= ENSP00000509639.1:n.*1005A=
ENST00000688812.1:c.756A= ENSP00000510658.1:p.Pro252=
ENST00000689218.1:n.985A=
ENST00000689484.1:c.-220-20746A= ENSP00000509884.1:n.-220-20746A=
ENST00000689797.1:c.-220-20746A= ENSP00000510689.1:n.-220-20746A=
ENST00000690544.1:c.756A= ENSP00000508989.1:p.Pro252=
ENST00000692038.1:c.*1005A= ENSP00000509220.1:n.*1005A=
ENST00000692953.1:n.62+16011A=
ENST00000692979.1:c.756A= ENSP00000509849.1:p.Pro252=
ENST00000358913.10:c.756A= MANE Select ENSP00000351790.5:p.Pro252=
ENST00000354393.6:c.77+15393A= ENSP00000346369.2:n.77+15393A=
ENST00000358913.9:c.756A= ENSP00000351790.5:p.Pro252=
ENST00000373675.3:c.756A= ENSP00000362779.3:p.Pro252=
ENST00000540630.5:c.756A= ENSP00000441668.2:p.Pro252=
ENST00000613327.4:c.-367A= ENSP00000480757.1:n.-367A=
NM_001256267.1:c.756A= NP_001243196.1:p.Pro252=
NM_001256268.1:c.-367A= NP_001243197.1:n.-367A=
NM_032578.3:c.756A= , LRG_410t1:c.756A= NP_115967.2:p.Pro252=
NR_045662.3:n.329+15393A=
NR_045663.3:n.1048A=
XM_006718043.2:c.756A= XP_006718106.1:p.Pro252=
XM_011540292.1:c.756A= XP_011538594.1:p.Pro252=
XM_017016833.1:c.834A= XP_016872322.1:p.Pro278=
XM_017016834.2:c.756A= XP_016872323.1:p.Pro252=
XM_024448236.1:c.-221+16011A= XP_024304004.1:n.-221+16011A=
NR_045662.4:n.439+15393A=
NR_045663.4:n.993A=
NM_001256267.2:c.756A= NP_001243196.1:p.Pro252=
NM_001256268.2:c.-367A= NP_001243197.1:n.-367A=
NM_032578.4:c.756A= MANE Select NP_115967.2:p.Pro252=