Canonical Allele Identifier: CA2831039288

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166315del , CM000672.2:g.68166315del	GRCh38
NC_000010.10:g.69926072del , CM000672.1:g.69926072del	GRCh37
NC_000010.9:g.69596078del	NCBI36
NG_032118.1:g.65199del , LRG_410:g.65199del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.797del	ENSP00000346369.2:p.Asn266ThrfsTer?
ENST00000373675.4:c.1622del	ENSP00000362779.4:p.Asn541ThrfsTer?
ENST00000540630.6:c.1676del	ENSP00000441668.3:p.Asn559ThrfsTer?
ENST00000613327.5:c.1622del	ENSP00000480757.2:p.Asn541ThrfsTer?
ENST00000687572.1:c.500del	ENSP00000510427.1:p.Asn167ThrfsTer?
ENST00000687705.1:c.*1871del	ENSP00000509639.1:n.*1871del
ENST00000688812.1:c.1598del	ENSP00000510658.1:p.Asn533ThrfsTer?
ENST00000689002.1:n.674del
ENST00000690544.1:c.*893del	ENSP00000508989.1:n.*893del
ENST00000358913.10:c.1622del MANE Select	ENSP00000351790.5:p.Asn541ThrfsTer?
ENST00000354393.6:c.797del	ENSP00000346369.2:p.Asn266ThrfsTer?
ENST00000358913.9:c.1622del	ENSP00000351790.5:p.Asn541ThrfsTer?
ENST00000540630.5:c.1622del	ENSP00000441668.2:p.Asn541ThrfsTer?
ENST00000613327.4:c.740del	ENSP00000480757.1:p.Asn247ThrfsTer?
NM_001256267.1:c.1622del	NP_001243196.1:p.Asn541ThrfsTer?
NM_001256268.1:c.740del	NP_001243197.1:p.Asn247ThrfsTer?
NM_032578.3:c.1622del , LRG_410t1:c.1622del	NP_115967.2:p.Asn541ThrfsTer?
NR_045662.3:n.1049del
NR_045663.3:n.1890del
XM_006718043.2:c.1676del	XP_006718106.1:p.Asn559ThrfsTer?
XM_011540292.1:c.1652del	XP_011538594.1:p.Asn551ThrfsTer?
XM_017016833.1:c.1700del	XP_016872322.1:p.Asn567ThrfsTer?
XM_017016834.2:c.1622del	XP_016872323.1:p.Asn541ThrfsTer?
XM_024448236.1:c.500del	XP_024304004.1:p.Asn167ThrfsTer?
NR_045662.4:n.1159del
NR_045663.4:n.1835del
NM_001256267.2:c.1622del	NP_001243196.1:p.Asn541ThrfsTer?
NM_001256268.2:c.740del	NP_001243197.1:p.Asn247ThrfsTer?
NM_032578.4:c.1622del MANE Select	NP_115967.2:p.Asn541ThrfsTer?