Canonical Allele Identifier: CA1917215606

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68165803C= , CM000672.2:g.68165803C=	GRCh38
NC_000010.10:g.69925560C= , CM000672.1:g.69925560C=	GRCh37
NC_000010.9:g.69595566C=	NCBI36
NG_032118.1:g.64687C= , LRG_410:g.64687C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.760C=	ENSP00000346369.2:p.Gln254=
ENST00000373675.4:c.1585C=	ENSP00000362779.4:p.Gln529=
ENST00000540630.6:c.1639C=	ENSP00000441668.3:p.Gln547=
ENST00000613327.5:c.1585C=	ENSP00000480757.2:p.Gln529=
ENST00000687572.1:c.463C=	ENSP00000510427.1:p.Gln155=
ENST00000687705.1:c.*1834C=	ENSP00000509639.1:n.*1834C=
ENST00000688812.1:c.1561C=	ENSP00000510658.1:p.Gln521=
ENST00000689002.1:n.637C=
ENST00000690544.1:c.*856C=	ENSP00000508989.1:n.*856C=
ENST00000358913.10:c.1585C= MANE Select	ENSP00000351790.5:p.Gln529=
ENST00000354393.6:c.760C=	ENSP00000346369.2:p.Gln254=
ENST00000358913.9:c.1585C=	ENSP00000351790.5:p.Gln529=
ENST00000540630.5:c.1585C=	ENSP00000441668.2:p.Gln529=
ENST00000613327.4:c.703C=	ENSP00000480757.1:p.Gln235=
NM_001256267.1:c.1585C=	NP_001243196.1:p.Gln529=
NM_001256268.1:c.703C=	NP_001243197.1:p.Gln235=
NM_032578.3:c.1585C= , LRG_410t1:c.1585C=	NP_115967.2:p.Gln529=
NR_045662.3:n.1012C=
NR_045663.3:n.1853C=
XM_006718043.2:c.1639C=	XP_006718106.1:p.Gln547=
XM_011540292.1:c.1615C=	XP_011538594.1:p.Gln539=
XM_017016833.1:c.1663C=	XP_016872322.1:p.Gln555=
XM_017016834.2:c.1585C=	XP_016872323.1:p.Gln529=
XM_024448236.1:c.463C=	XP_024304004.1:p.Gln155=
NR_045662.4:n.1122C=
NR_045663.4:n.1798C=
NM_001256267.2:c.1585C=	NP_001243196.1:p.Gln529=
NM_001256268.2:c.703C=	NP_001243197.1:p.Gln235=
NM_032578.4:c.1585C= MANE Select	NP_115967.2:p.Gln529=