Canonical Allele Identifier: CA1917215865

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166472G= , CM000672.2:g.68166472G=	GRCh38
NC_000010.10:g.69926229G= , CM000672.1:g.69926229G=	GRCh37
NC_000010.9:g.69596235G=	NCBI36
NG_032118.1:g.65356G= , LRG_410:g.65356G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.954G=	ENSP00000346369.2:p.Arg318=
ENST00000373675.4:c.1779G=	ENSP00000362779.4:p.Arg593=
ENST00000540630.6:c.1833G=	ENSP00000441668.3:p.Arg611=
ENST00000613327.5:c.1779G=	ENSP00000480757.2:p.Arg593=
ENST00000687572.1:c.657G=	ENSP00000510427.1:p.Arg219=
ENST00000688812.1:c.1755G=	ENSP00000510658.1:p.Arg585=
ENST00000690544.1:c.*1050G=	ENSP00000508989.1:n.*1050G=
ENST00000358913.10:c.1779G= MANE Select	ENSP00000351790.5:p.Arg593=
ENST00000354393.6:c.954G=	ENSP00000346369.2:p.Arg318=
ENST00000358913.9:c.1779G=	ENSP00000351790.5:p.Arg593=
ENST00000540630.5:c.1779G=	ENSP00000441668.2:p.Arg593=
ENST00000613327.4:c.897G=	ENSP00000480757.1:p.Arg299=
NM_001256267.1:c.1779G=	NP_001243196.1:p.Arg593=
NM_001256268.1:c.897G=	NP_001243197.1:p.Arg299=
NM_032578.3:c.1779G= , LRG_410t1:c.1779G=	NP_115967.2:p.Arg593=
NR_045662.3:n.1206G=
NR_045663.3:n.2047G=
XM_006718043.2:c.1833G=	XP_006718106.1:p.Arg611=
XM_011540292.1:c.1809G=	XP_011538594.1:p.Arg603=
XM_017016833.1:c.1857G=	XP_016872322.1:p.Arg619=
XM_017016834.2:c.1779G=	XP_016872323.1:p.Arg593=
XM_024448236.1:c.657G=	XP_024304004.1:p.Arg219=
NR_045662.4:n.1316G=
NR_045663.4:n.1992G=
NM_001256267.2:c.1779G=	NP_001243196.1:p.Arg593=
NM_001256268.2:c.897G=	NP_001243197.1:p.Arg299=
NM_032578.4:c.1779G= MANE Select	NP_115967.2:p.Arg593=