Canonical Allele Identifier: CA376859047

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199425_68199426del , CM000672.2:g.68199425_68199426del	GRCh38
NC_000010.10:g.69959182_69959183del , CM000672.1:g.69959182_69959183del	GRCh37
NC_000010.9:g.69629188_69629189del	NCBI36
NG_032118.1:g.98309_98310del , LRG_410:g.98309_98310del

Transcript Alleles

HGVS	Amino-acid Change
NM_032578.4:c.3343_3344del MANE Select	NP_115967.2:p.Pro1115ArgfsTer19
ENST00000358913.10:c.3343_3344del MANE Select	ENSP00000351790.5:p.Pro1115ArgfsTer19
NM_001256267.1:c.3343_3344del	NP_001243196.1:p.Pro1115ArgfsTer19
NM_001256267.2:c.3343_3344del	NP_001243196.1:p.Pro1115ArgfsTer19
NM_001256268.1:c.2461_2462del	NP_001243197.1:p.Pro821ArgfsTer19
NM_001256268.2:c.2461_2462del	NP_001243197.1:p.Pro821ArgfsTer19
NM_032578.3:c.3343_3344del , LRG_410t1:c.3343_3344del	NP_115967.2:p.Pro1115ArgfsTer19
NR_045662.3:n.2770_2771del
NR_045662.4:n.2880_2881del
NR_045663.3:n.3472_3473del
NR_045663.4:n.3417_3418del
ENST00000354393.6:c.2518_2519del	ENSP00000346369.2:p.Pro840ArgfsTer19
ENST00000354393.7:c.2518_2519del	ENSP00000346369.2:p.Pro840ArgfsTer19
ENST00000358913.9:c.3343_3344del	ENSP00000351790.5:p.Pro1115ArgfsTer19
ENST00000540630.5:c.3343_3344del	ENSP00000441668.2:p.Pro1115ArgfsTer19
ENST00000540630.6:c.3397_3398del	ENSP00000441668.3:p.Pro1133ArgfsTer19
ENST00000613327.4:c.2461_2462del	ENSP00000480757.1:p.Pro821ArgfsTer19
ENST00000613327.5:c.3343_3344del	ENSP00000480757.2:p.Pro1115ArgfsTer19
ENST00000688812.1:c.*606_*607del	ENSP00000510658.1:n.*606_*607del
ENST00000690544.1:c.*2614_*2615del	ENSP00000508989.1:n.*2614_*2615del
XM_006718043.2:c.3397_3398del	XP_006718106.1:p.Pro1133ArgfsTer19
XM_011540292.1:c.3373_3374del	XP_011538594.1:p.Pro1125ArgfsTer19
XM_017016833.1:c.3421_3422del	XP_016872322.1:p.Pro1141ArgfsTer19
XM_017016834.2:c.3343_3344del	XP_016872323.1:p.Pro1115ArgfsTer19
XM_024448236.1:c.2221_2222del	XP_024304004.1:p.Pro741ArgfsTer19
XR_946029.1:n.1804-151_1804-150del