Canonical Allele Identifier: CA1917226436

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68197362C= , CM000672.2:g.68197362C=	GRCh38
NC_000010.10:g.69957119C= , CM000672.1:g.69957119C=	GRCh37
NC_000010.9:g.69627125C=	NCBI36
NG_032118.1:g.96246C= , LRG_410:g.96246C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2344C=	ENSP00000346369.2:p.Arg782=
ENST00000540630.6:c.3223C=	ENSP00000441668.3:p.Arg1075=
ENST00000613327.5:c.3169C=	ENSP00000480757.2:p.Arg1057=
ENST00000688812.1:c.*432C=	ENSP00000510658.1:n.*432C=
ENST00000690544.1:c.*2440C=	ENSP00000508989.1:n.*2440C=
ENST00000358913.10:c.3169C= MANE Select	ENSP00000351790.5:p.Arg1057=
ENST00000354393.6:c.2344C=	ENSP00000346369.2:p.Arg782=
ENST00000358913.9:c.3169C=	ENSP00000351790.5:p.Arg1057=
ENST00000540630.5:c.3169C=	ENSP00000441668.2:p.Arg1057=
ENST00000613327.4:c.2287C=	ENSP00000480757.1:p.Arg763=
NM_001256267.1:c.3169C=	NP_001243196.1:p.Arg1057=
NM_001256268.1:c.2287C=	NP_001243197.1:p.Arg763=
NM_032578.3:c.3169C= , LRG_410t1:c.3169C=	NP_115967.2:p.Arg1057=
NR_045662.3:n.2596C=
NR_045663.3:n.3298C=
XM_006718043.2:c.3223C=	XP_006718106.1:p.Arg1075=
XM_011540292.1:c.3199C=	XP_011538594.1:p.Arg1067=
XM_017016833.1:c.3247C=	XP_016872322.1:p.Arg1083=
XM_017016834.2:c.3169C=	XP_016872323.1:p.Arg1057=
XM_024448236.1:c.2047C=	XP_024304004.1:p.Arg683=
NR_045662.4:n.2706C=
NR_045663.4:n.3243C=
NM_001256267.2:c.3169C=	NP_001243196.1:p.Arg1057=
NM_001256268.2:c.2287C=	NP_001243197.1:p.Arg763=
NM_032578.4:c.3169C= MANE Select	NP_115967.2:p.Arg1057=