Canonical Allele Identifier: CA1917232490
Gene: MYPN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68210513G= , CM000672.2:g.68210513G= GRCh38
NC_000010.10:g.69970270G= , CM000672.1:g.69970270G= GRCh37
NC_000010.9:g.69640276G= NCBI36
NG_032118.1:g.109397G= , LRG_410:g.109397G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000354393.7:c.*58G= ENSP00000346369.2:n.*58G=
ENST00000540630.6:c.*58G= ENSP00000441668.3:n.*58G=
ENST00000613327.5:c.*58G= ENSP00000480757.2:n.*58G=
ENST00000688812.1:c.*1284G= ENSP00000510658.1:n.*1284G=
ENST00000690544.1:c.*3292G= ENSP00000508989.1:n.*3292G=
ENST00000358913.10:c.*58G= MANE Select ENSP00000351790.5:n.*58G=
ENST00000354393.6:c.*58G= ENSP00000346369.2:n.*58G=
ENST00000358913.9:c.*58G= ENSP00000351790.5:n.*58G=
ENST00000540630.5:c.*58G= ENSP00000441668.2:n.*58G=
ENST00000613327.4:c.*58G= ENSP00000480757.1:n.*58G=
NM_001256267.1:c.*58G= NP_001243196.1:n.*58G=
NM_001256268.1:c.*58G= NP_001243197.1:n.*58G=
NM_032578.3:c.*58G= , LRG_410t1:c.*58G= NP_115967.2:n.*58G=
NR_045662.3:n.3448G=
NR_045663.3:n.4150G=
XM_006718043.2:c.*58G= XP_006718106.1:n.*58G=
XM_011540292.1:c.*58G= XP_011538594.1:n.*58G=
XR_946029.1:n.1574+4775C=
XM_017016833.1:c.*58G= XP_016872322.1:n.*58G=
XM_017016834.2:c.*58G= XP_016872323.1:n.*58G=
XM_024448236.1:c.*58G= XP_024304004.1:n.*58G=
NR_045662.4:n.3558G=
NR_045663.4:n.4095G=
NM_001256267.2:c.*58G= NP_001243196.1:n.*58G=
NM_001256268.2:c.*58G= NP_001243197.1:n.*58G=
NM_032578.4:c.*58G= MANE Select NP_115967.2:n.*58G=