Canonical Allele Identifier: CA1917226438

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68197366T= , CM000672.2:g.68197366T=	GRCh38
NC_000010.10:g.69957123T= , CM000672.1:g.69957123T=	GRCh37
NC_000010.9:g.69627129T=	NCBI36
NG_032118.1:g.96250T= , LRG_410:g.96250T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2348T=	ENSP00000346369.2:p.Val783=
ENST00000540630.6:c.3227T=	ENSP00000441668.3:p.Val1076=
ENST00000613327.5:c.3173T=	ENSP00000480757.2:p.Val1058=
ENST00000688812.1:c.*436T=	ENSP00000510658.1:n.*436T=
ENST00000690544.1:c.*2444T=	ENSP00000508989.1:n.*2444T=
ENST00000358913.10:c.3173T= MANE Select	ENSP00000351790.5:p.Val1058=
ENST00000354393.6:c.2348T=	ENSP00000346369.2:p.Val783=
ENST00000358913.9:c.3173T=	ENSP00000351790.5:p.Val1058=
ENST00000540630.5:c.3173T=	ENSP00000441668.2:p.Val1058=
ENST00000613327.4:c.2291T=	ENSP00000480757.1:p.Val764=
NM_001256267.1:c.3173T=	NP_001243196.1:p.Val1058=
NM_001256268.1:c.2291T=	NP_001243197.1:p.Val764=
NM_032578.3:c.3173T= , LRG_410t1:c.3173T=	NP_115967.2:p.Val1058=
NR_045662.3:n.2600T=
NR_045663.3:n.3302T=
XM_006718043.2:c.3227T=	XP_006718106.1:p.Val1076=
XM_011540292.1:c.3203T=	XP_011538594.1:p.Val1068=
XM_017016833.1:c.3251T=	XP_016872322.1:p.Val1084=
XM_017016834.2:c.3173T=	XP_016872323.1:p.Val1058=
XM_024448236.1:c.2051T=	XP_024304004.1:p.Val684=
NR_045662.4:n.2710T=
NR_045663.4:n.3247T=
NM_001256267.2:c.3173T=	NP_001243196.1:p.Val1058=
NM_001256268.2:c.2291T=	NP_001243197.1:p.Val764=
NM_032578.4:c.3173T= MANE Select	NP_115967.2:p.Val1058=