Canonical Allele Identifier: CA2574591122

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166643del , CM000672.2:g.68166643del	GRCh38
NC_000010.10:g.69926400del , CM000672.1:g.69926400del	GRCh37
NC_000010.9:g.69596406del	NCBI36
NG_032118.1:g.65527del , LRG_410:g.65527del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1125del	ENSP00000346369.2:p.Pro376GlnfsTer?
ENST00000373675.4:c.1950del	ENSP00000362779.4:p.Pro651GlnfsTer10
ENST00000540630.6:c.2004del	ENSP00000441668.3:p.Pro669GlnfsTer?
ENST00000613327.5:c.1950del	ENSP00000480757.2:p.Pro651GlnfsTer?
ENST00000687572.1:c.828del	ENSP00000510427.1:p.Pro277GlnfsTer?
ENST00000688812.1:c.1926del	ENSP00000510658.1:p.Pro643GlnfsTer?
ENST00000690544.1:c.*1221del	ENSP00000508989.1:n.*1221del
ENST00000358913.10:c.1950del MANE Select	ENSP00000351790.5:p.Pro651GlnfsTer?
ENST00000354393.6:c.1125del	ENSP00000346369.2:p.Pro376GlnfsTer?
ENST00000358913.9:c.1950del	ENSP00000351790.5:p.Pro651GlnfsTer?
ENST00000540630.5:c.1950del	ENSP00000441668.2:p.Pro651GlnfsTer?
ENST00000613327.4:c.1068del	ENSP00000480757.1:p.Pro357GlnfsTer?
NM_001256267.1:c.1950del	NP_001243196.1:p.Pro651GlnfsTer?
NM_001256268.1:c.1068del	NP_001243197.1:p.Pro357GlnfsTer?
NM_032578.3:c.1950del , LRG_410t1:c.1950del	NP_115967.2:p.Pro651GlnfsTer?
NR_045662.3:n.1377del
NR_045663.3:n.2218del
XM_006718043.2:c.2004del	XP_006718106.1:p.Pro669GlnfsTer?
XM_011540292.1:c.1980del	XP_011538594.1:p.Pro661GlnfsTer?
XM_017016833.1:c.2028del	XP_016872322.1:p.Pro677GlnfsTer?
XM_017016834.2:c.1950del	XP_016872323.1:p.Pro651GlnfsTer?
XM_024448236.1:c.828del	XP_024304004.1:p.Pro277GlnfsTer?
NR_045662.4:n.1487del
NR_045663.4:n.2163del
NM_001256267.2:c.1950del	NP_001243196.1:p.Pro651GlnfsTer?
NM_001256268.2:c.1068del	NP_001243197.1:p.Pro357GlnfsTer?
NM_032578.4:c.1950del MANE Select	NP_115967.2:p.Pro651GlnfsTer?