Canonical Allele Identifier: CA1917215831

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166393C= , CM000672.2:g.68166393C=	GRCh38
NC_000010.10:g.69926150C= , CM000672.1:g.69926150C=	GRCh37
NC_000010.9:g.69596156C=	NCBI36
NG_032118.1:g.65277C= , LRG_410:g.65277C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.875C=	ENSP00000346369.2:p.Pro292=
ENST00000373675.4:c.1700C=	ENSP00000362779.4:p.Pro567=
ENST00000540630.6:c.1754C=	ENSP00000441668.3:p.Pro585=
ENST00000613327.5:c.1700C=	ENSP00000480757.2:p.Pro567=
ENST00000687572.1:c.578C=	ENSP00000510427.1:p.Pro193=
ENST00000688812.1:c.1676C=	ENSP00000510658.1:p.Pro559=
ENST00000689002.1:n.752C=
ENST00000690544.1:c.*971C=	ENSP00000508989.1:n.*971C=
ENST00000358913.10:c.1700C= MANE Select	ENSP00000351790.5:p.Pro567=
ENST00000354393.6:c.875C=	ENSP00000346369.2:p.Pro292=
ENST00000358913.9:c.1700C=	ENSP00000351790.5:p.Pro567=
ENST00000540630.5:c.1700C=	ENSP00000441668.2:p.Pro567=
ENST00000613327.4:c.818C=	ENSP00000480757.1:p.Pro273=
NM_001256267.1:c.1700C=	NP_001243196.1:p.Pro567=
NM_001256268.1:c.818C=	NP_001243197.1:p.Pro273=
NM_032578.3:c.1700C= , LRG_410t1:c.1700C=	NP_115967.2:p.Pro567=
NR_045662.3:n.1127C=
NR_045663.3:n.1968C=
XM_006718043.2:c.1754C=	XP_006718106.1:p.Pro585=
XM_011540292.1:c.1730C=	XP_011538594.1:p.Pro577=
XM_017016833.1:c.1778C=	XP_016872322.1:p.Pro593=
XM_017016834.2:c.1700C=	XP_016872323.1:p.Pro567=
XM_024448236.1:c.578C=	XP_024304004.1:p.Pro193=
NR_045662.4:n.1237C=
NR_045663.4:n.1913C=
NM_001256267.2:c.1700C=	NP_001243196.1:p.Pro567=
NM_001256268.2:c.818C=	NP_001243197.1:p.Pro273=
NM_032578.4:c.1700C= MANE Select	NP_115967.2:p.Pro567=