Canonical Allele Identifier: CA1917227422

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199497C= , CM000672.2:g.68199497C=	GRCh38
NC_000010.10:g.69959254C= , CM000672.1:g.69959254C=	GRCh37
NC_000010.9:g.69629260C=	NCBI36
NG_032118.1:g.98381C= , LRG_410:g.98381C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2590C=	ENSP00000346369.2:p.Arg864=
ENST00000540630.6:c.3469C=	ENSP00000441668.3:p.Arg1157=
ENST00000613327.5:c.3415C=	ENSP00000480757.2:p.Arg1139=
ENST00000688812.1:c.*678C=	ENSP00000510658.1:n.*678C=
ENST00000690544.1:c.*2686C=	ENSP00000508989.1:n.*2686C=
ENST00000358913.10:c.3415C= MANE Select	ENSP00000351790.5:p.Arg1139=
ENST00000354393.6:c.2590C=	ENSP00000346369.2:p.Arg864=
ENST00000358913.9:c.3415C=	ENSP00000351790.5:p.Arg1139=
ENST00000540630.5:c.3415C=	ENSP00000441668.2:p.Arg1139=
ENST00000613327.4:c.2533C=	ENSP00000480757.1:p.Arg845=
NM_001256267.1:c.3415C=	NP_001243196.1:p.Arg1139=
NM_001256268.1:c.2533C=	NP_001243197.1:p.Arg845=
NM_032578.3:c.3415C= , LRG_410t1:c.3415C=	NP_115967.2:p.Arg1139=
NR_045662.3:n.2842C=
NR_045663.3:n.3544C=
XM_006718043.2:c.3469C=	XP_006718106.1:p.Arg1157=
XM_011540292.1:c.3445C=	XP_011538594.1:p.Arg1149=
XR_946029.1:n.1804-222G=
XM_017016833.1:c.3493C=	XP_016872322.1:p.Arg1165=
XM_017016834.2:c.3415C=	XP_016872323.1:p.Arg1139=
XM_024448236.1:c.2293C=	XP_024304004.1:p.Arg765=
NR_045662.4:n.2952C=
NR_045663.4:n.3489C=
NM_001256267.2:c.3415C=	NP_001243196.1:p.Arg1139=
NM_001256268.2:c.2533C=	NP_001243197.1:p.Arg845=
NM_032578.4:c.3415C= MANE Select	NP_115967.2:p.Arg1139=