Canonical Allele Identifier: CA2722304604

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199498del , CM000672.2:g.68199498del	GRCh38
NC_000010.10:g.69959255del , CM000672.1:g.69959255del	GRCh37
NC_000010.9:g.69629261del	NCBI36
NG_032118.1:g.98382del , LRG_410:g.98382del

Transcript Alleles

HGVS	Amino-acid Change
NM_032578.4:c.3416del MANE Select	NP_115967.2:p.Arg1139ProfsTer25
ENST00000358913.10:c.3416del MANE Select	ENSP00000351790.5:p.Arg1139ProfsTer25
NM_001256267.1:c.3416del	NP_001243196.1:p.Arg1139ProfsTer25
NM_001256267.2:c.3416del	NP_001243196.1:p.Arg1139ProfsTer25
NM_001256268.1:c.2534del	NP_001243197.1:p.Arg845ProfsTer25
NM_001256268.2:c.2534del	NP_001243197.1:p.Arg845ProfsTer25
NM_032578.3:c.3416del , LRG_410t1:c.3416del	NP_115967.2:p.Arg1139ProfsTer25
NR_045662.3:n.2843del
NR_045662.4:n.2953del
NR_045663.3:n.3545del
NR_045663.4:n.3490del
ENST00000354393.6:c.2591del	ENSP00000346369.2:p.Arg864ProfsTer25
ENST00000354393.7:c.2591del	ENSP00000346369.2:p.Arg864ProfsTer25
ENST00000358913.9:c.3416del	ENSP00000351790.5:p.Arg1139ProfsTer25
ENST00000540630.5:c.3416del	ENSP00000441668.2:p.Arg1139ProfsTer25
ENST00000540630.6:c.3470del	ENSP00000441668.3:p.Arg1157ProfsTer25
ENST00000613327.4:c.2534del	ENSP00000480757.1:p.Arg845ProfsTer25
ENST00000613327.5:c.3416del	ENSP00000480757.2:p.Arg1139ProfsTer25
ENST00000688812.1:c.*679del	ENSP00000510658.1:n.*679del
ENST00000690544.1:c.*2687del	ENSP00000508989.1:n.*2687del
XM_006718043.2:c.3470del	XP_006718106.1:p.Arg1157ProfsTer25
XM_011540292.1:c.3446del	XP_011538594.1:p.Arg1149ProfsTer25
XM_017016833.1:c.3494del	XP_016872322.1:p.Arg1165ProfsTer25
XM_017016834.2:c.3416del	XP_016872323.1:p.Arg1139ProfsTer25
XM_024448236.1:c.2294del	XP_024304004.1:p.Arg765ProfsTer25
XR_946029.1:n.1804-223del