Canonical Allele Identifier: CA1917215797

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166298T= , CM000672.2:g.68166298T=	GRCh38
NC_000010.10:g.69926055T= , CM000672.1:g.69926055T=	GRCh37
NC_000010.9:g.69596061T=	NCBI36
NG_032118.1:g.65182T= , LRG_410:g.65182T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.780T=	ENSP00000346369.2:p.Asn260=
ENST00000373675.4:c.1605T=	ENSP00000362779.4:p.Asn535=
ENST00000540630.6:c.1659T=	ENSP00000441668.3:p.Asn553=
ENST00000613327.5:c.1605T=	ENSP00000480757.2:p.Asn535=
ENST00000687572.1:c.483T=	ENSP00000510427.1:p.Asn161=
ENST00000687705.1:c.*1854T=	ENSP00000509639.1:n.*1854T=
ENST00000688812.1:c.1581T=	ENSP00000510658.1:p.Asn527=
ENST00000689002.1:n.657T=
ENST00000690544.1:c.*876T=	ENSP00000508989.1:n.*876T=
ENST00000358913.10:c.1605T= MANE Select	ENSP00000351790.5:p.Asn535=
ENST00000354393.6:c.780T=	ENSP00000346369.2:p.Asn260=
ENST00000358913.9:c.1605T=	ENSP00000351790.5:p.Asn535=
ENST00000540630.5:c.1605T=	ENSP00000441668.2:p.Asn535=
ENST00000613327.4:c.723T=	ENSP00000480757.1:p.Asn241=
NM_001256267.1:c.1605T=	NP_001243196.1:p.Asn535=
NM_001256268.1:c.723T=	NP_001243197.1:p.Asn241=
NM_032578.3:c.1605T= , LRG_410t1:c.1605T=	NP_115967.2:p.Asn535=
NR_045662.3:n.1032T=
NR_045663.3:n.1873T=
XM_006718043.2:c.1659T=	XP_006718106.1:p.Asn553=
XM_011540292.1:c.1635T=	XP_011538594.1:p.Asn545=
XM_017016833.1:c.1683T=	XP_016872322.1:p.Asn561=
XM_017016834.2:c.1605T=	XP_016872323.1:p.Asn535=
XM_024448236.1:c.483T=	XP_024304004.1:p.Asn161=
NR_045662.4:n.1142T=
NR_045663.4:n.1818T=
NM_001256267.2:c.1605T=	NP_001243196.1:p.Asn535=
NM_001256268.2:c.723T=	NP_001243197.1:p.Asn241=
NM_032578.4:c.1605T= MANE Select	NP_115967.2:p.Asn535=