Canonical Allele Identifier: CA1917215945
Gene: MYPN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68166659C= , CM000672.2:g.68166659C= GRCh38
NC_000010.10:g.69926416C= , CM000672.1:g.69926416C= GRCh37
NC_000010.9:g.69596422C= NCBI36
NG_032118.1:g.65543C= , LRG_410:g.65543C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000354393.7:c.1141C= ENSP00000346369.2:p.Pro381=
ENST00000373675.4:c.1966C= ENSP00000362779.4:p.Pro656=
ENST00000540630.6:c.2020C= ENSP00000441668.3:p.Pro674=
ENST00000613327.5:c.1966C= ENSP00000480757.2:p.Pro656=
ENST00000687572.1:c.844C= ENSP00000510427.1:p.Pro282=
ENST00000688812.1:c.1942C= ENSP00000510658.1:p.Pro648=
ENST00000690544.1:c.*1237C= ENSP00000508989.1:n.*1237C=
ENST00000358913.10:c.1966C= MANE Select ENSP00000351790.5:p.Pro656=
ENST00000354393.6:c.1141C= ENSP00000346369.2:p.Pro381=
ENST00000358913.9:c.1966C= ENSP00000351790.5:p.Pro656=
ENST00000540630.5:c.1966C= ENSP00000441668.2:p.Pro656=
ENST00000613327.4:c.1084C= ENSP00000480757.1:p.Pro362=
NM_001256267.1:c.1966C= NP_001243196.1:p.Pro656=
NM_001256268.1:c.1084C= NP_001243197.1:p.Pro362=
NM_032578.3:c.1966C= , LRG_410t1:c.1966C= NP_115967.2:p.Pro656=
NR_045662.3:n.1393C=
NR_045663.3:n.2234C=
XM_006718043.2:c.2020C= XP_006718106.1:p.Pro674=
XM_011540292.1:c.1996C= XP_011538594.1:p.Pro666=
XM_017016833.1:c.2044C= XP_016872322.1:p.Pro682=
XM_017016834.2:c.1966C= XP_016872323.1:p.Pro656=
XM_024448236.1:c.844C= XP_024304004.1:p.Pro282=
NR_045662.4:n.1503C=
NR_045663.4:n.2179C=
NM_001256267.2:c.1966C= NP_001243196.1:p.Pro656=
NM_001256268.2:c.1084C= NP_001243197.1:p.Pro362=
NM_032578.4:c.1966C= MANE Select NP_115967.2:p.Pro656=