Canonical Allele Identifier: CA2722282867

Gene: MYPN

Linked Data

• dbSNP Id: rs2134167857

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166340del , CM000672.2:g.68166340del	GRCh38
NC_000010.10:g.69926097del , CM000672.1:g.69926097del	GRCh37
NC_000010.9:g.69596103del	NCBI36
NG_032118.1:g.65224del , LRG_410:g.65224del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.822del	ENSP00000346369.2:p.Thr275ProfsTer?
ENST00000373675.4:c.1647del	ENSP00000362779.4:p.Thr550ProfsTer?
ENST00000540630.6:c.1701del	ENSP00000441668.3:p.Thr568ProfsTer?
ENST00000613327.5:c.1647del	ENSP00000480757.2:p.Thr550ProfsTer?
ENST00000687572.1:c.525del	ENSP00000510427.1:p.Thr176ProfsTer?
ENST00000687705.1:c.*1896del	ENSP00000509639.1:n.*1896del
ENST00000688812.1:c.1623del	ENSP00000510658.1:p.Thr542ProfsTer?
ENST00000689002.1:n.699del
ENST00000690544.1:c.*918del	ENSP00000508989.1:n.*918del
ENST00000358913.10:c.1647del MANE Select	ENSP00000351790.5:p.Thr550ProfsTer?
ENST00000354393.6:c.822del	ENSP00000346369.2:p.Thr275ProfsTer?
ENST00000358913.9:c.1647del	ENSP00000351790.5:p.Thr550ProfsTer?
ENST00000540630.5:c.1647del	ENSP00000441668.2:p.Thr550ProfsTer?
ENST00000613327.4:c.765del	ENSP00000480757.1:p.Thr256ProfsTer?
NM_001256267.1:c.1647del	NP_001243196.1:p.Thr550ProfsTer?
NM_001256268.1:c.765del	NP_001243197.1:p.Thr256ProfsTer?
NM_032578.3:c.1647del , LRG_410t1:c.1647del	NP_115967.2:p.Thr550ProfsTer?
NR_045662.3:n.1074del
NR_045663.3:n.1915del
XM_006718043.2:c.1701del	XP_006718106.1:p.Thr568ProfsTer?
XM_011540292.1:c.1677del	XP_011538594.1:p.Thr560ProfsTer?
XM_017016833.1:c.1725del	XP_016872322.1:p.Thr576ProfsTer?
XM_017016834.2:c.1647del	XP_016872323.1:p.Thr550ProfsTer?
XM_024448236.1:c.525del	XP_024304004.1:p.Thr176ProfsTer?
NR_045662.4:n.1184del
NR_045663.4:n.1860del
NM_001256267.2:c.1647del	NP_001243196.1:p.Thr550ProfsTer?
NM_001256268.2:c.765del	NP_001243197.1:p.Thr256ProfsTer?
NM_032578.4:c.1647del MANE Select	NP_115967.2:p.Thr550ProfsTer?