Canonical Allele Identifier: CA2574591120

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166603del , CM000672.2:g.68166603del	GRCh38
NC_000010.10:g.69926360del , CM000672.1:g.69926360del	GRCh37
NC_000010.9:g.69596366del	NCBI36
NG_032118.1:g.65487del , LRG_410:g.65487del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1085del	ENSP00000346369.2:p.Thr362LysfsTer10
ENST00000373675.4:c.1910del	ENSP00000362779.4:p.Thr637LysfsTer10
ENST00000540630.6:c.1964del	ENSP00000441668.3:p.Thr655LysfsTer10
ENST00000613327.5:c.1910del	ENSP00000480757.2:p.Thr637LysfsTer10
ENST00000687572.1:c.788del	ENSP00000510427.1:p.Thr263LysfsTer10
ENST00000688812.1:c.1886del	ENSP00000510658.1:p.Thr629LysfsTer10
ENST00000690544.1:c.*1181del	ENSP00000508989.1:n.*1181del
ENST00000358913.10:c.1910del MANE Select	ENSP00000351790.5:p.Thr637LysfsTer10
ENST00000354393.6:c.1085del	ENSP00000346369.2:p.Thr362LysfsTer10
ENST00000358913.9:c.1910del	ENSP00000351790.5:p.Thr637LysfsTer10
ENST00000540630.5:c.1910del	ENSP00000441668.2:p.Thr637LysfsTer10
ENST00000613327.4:c.1028del	ENSP00000480757.1:p.Thr343LysfsTer10
NM_001256267.1:c.1910del	NP_001243196.1:p.Thr637LysfsTer10
NM_001256268.1:c.1028del	NP_001243197.1:p.Thr343LysfsTer10
NM_032578.3:c.1910del , LRG_410t1:c.1910del	NP_115967.2:p.Thr637LysfsTer10
NR_045662.3:n.1337del
NR_045663.3:n.2178del
XM_006718043.2:c.1964del	XP_006718106.1:p.Thr655LysfsTer10
XM_011540292.1:c.1940del	XP_011538594.1:p.Thr647LysfsTer10
XM_017016833.1:c.1988del	XP_016872322.1:p.Thr663LysfsTer10
XM_017016834.2:c.1910del	XP_016872323.1:p.Thr637LysfsTer10
XM_024448236.1:c.788del	XP_024304004.1:p.Thr263LysfsTer10
NR_045662.4:n.1447del
NR_045663.4:n.2123del
NM_001256267.2:c.1910del	NP_001243196.1:p.Thr637LysfsTer10
NM_001256268.2:c.1028del	NP_001243197.1:p.Thr343LysfsTer10
NM_032578.4:c.1910del MANE Select	NP_115967.2:p.Thr637LysfsTer10