Canonical Allele Identifier: CA2609373568

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199426dup , CM000672.2:g.68199426dup	GRCh38
NC_000010.10:g.69959183dup , CM000672.1:g.69959183dup	GRCh37
NC_000010.9:g.69629189dup	NCBI36
NG_032118.1:g.98310dup , LRG_410:g.98310dup

Transcript Alleles

HGVS	Amino-acid Change
NM_032578.4:c.3344dup MANE Select	NP_115967.2:p.Asp1116ArgfsTer19
ENST00000358913.10:c.3344dup MANE Select	ENSP00000351790.5:p.Asp1116ArgfsTer19
NM_001256267.1:c.3344dup	NP_001243196.1:p.Asp1116ArgfsTer19
NM_001256267.2:c.3344dup	NP_001243196.1:p.Asp1116ArgfsTer19
NM_001256268.1:c.2462dup	NP_001243197.1:p.Asp822ArgfsTer19
NM_001256268.2:c.2462dup	NP_001243197.1:p.Asp822ArgfsTer19
NM_032578.3:c.3344dup , LRG_410t1:c.3344dup	NP_115967.2:p.Asp1116ArgfsTer19
NR_045662.3:n.2771dup
NR_045662.4:n.2881dup
NR_045663.3:n.3473dup
NR_045663.4:n.3418dup
ENST00000354393.6:c.2519dup	ENSP00000346369.2:p.Asp841ArgfsTer19
ENST00000354393.7:c.2519dup	ENSP00000346369.2:p.Asp841ArgfsTer19
ENST00000358913.9:c.3344dup	ENSP00000351790.5:p.Asp1116ArgfsTer19
ENST00000540630.5:c.3344dup	ENSP00000441668.2:p.Asp1116ArgfsTer19
ENST00000540630.6:c.3398dup	ENSP00000441668.3:p.Asp1134ArgfsTer19
ENST00000613327.4:c.2462dup	ENSP00000480757.1:p.Asp822ArgfsTer19
ENST00000613327.5:c.3344dup	ENSP00000480757.2:p.Asp1116ArgfsTer19
ENST00000688812.1:c.*607dup	ENSP00000510658.1:n.*607dup
ENST00000690544.1:c.*2615dup	ENSP00000508989.1:n.*2615dup
XM_006718043.2:c.3398dup	XP_006718106.1:p.Asp1134ArgfsTer19
XM_011540292.1:c.3374dup	XP_011538594.1:p.Asp1126ArgfsTer19
XM_017016833.1:c.3422dup	XP_016872322.1:p.Asp1142ArgfsTer19
XM_017016834.2:c.3344dup	XP_016872323.1:p.Asp1116ArgfsTer19
XM_024448236.1:c.2222dup	XP_024304004.1:p.Asp742ArgfsTer19
XR_946029.1:n.1804-150dup