Canonical Allele Identifier: CA1917215825

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166374T= , CM000672.2:g.68166374T=	GRCh38
NC_000010.10:g.69926131T= , CM000672.1:g.69926131T=	GRCh37
NC_000010.9:g.69596137T=	NCBI36
NG_032118.1:g.65258T= , LRG_410:g.65258T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.856T=	ENSP00000346369.2:p.Ser286=
ENST00000373675.4:c.1681T=	ENSP00000362779.4:p.Ser561=
ENST00000540630.6:c.1735T=	ENSP00000441668.3:p.Ser579=
ENST00000613327.5:c.1681T=	ENSP00000480757.2:p.Ser561=
ENST00000687572.1:c.559T=	ENSP00000510427.1:p.Ser187=
ENST00000687705.1:c.*1930T=	ENSP00000509639.1:n.*1930T=
ENST00000688812.1:c.1657T=	ENSP00000510658.1:p.Ser553=
ENST00000689002.1:n.733T=
ENST00000690544.1:c.*952T=	ENSP00000508989.1:n.*952T=
ENST00000358913.10:c.1681T= MANE Select	ENSP00000351790.5:p.Ser561=
ENST00000354393.6:c.856T=	ENSP00000346369.2:p.Ser286=
ENST00000358913.9:c.1681T=	ENSP00000351790.5:p.Ser561=
ENST00000540630.5:c.1681T=	ENSP00000441668.2:p.Ser561=
ENST00000613327.4:c.799T=	ENSP00000480757.1:p.Ser267=
NM_001256267.1:c.1681T=	NP_001243196.1:p.Ser561=
NM_001256268.1:c.799T=	NP_001243197.1:p.Ser267=
NM_032578.3:c.1681T= , LRG_410t1:c.1681T=	NP_115967.2:p.Ser561=
NR_045662.3:n.1108T=
NR_045663.3:n.1949T=
XM_006718043.2:c.1735T=	XP_006718106.1:p.Ser579=
XM_011540292.1:c.1711T=	XP_011538594.1:p.Ser571=
XM_017016833.1:c.1759T=	XP_016872322.1:p.Ser587=
XM_017016834.2:c.1681T=	XP_016872323.1:p.Ser561=
XM_024448236.1:c.559T=	XP_024304004.1:p.Ser187=
NR_045662.4:n.1218T=
NR_045663.4:n.1894T=
NM_001256267.2:c.1681T=	NP_001243196.1:p.Ser561=
NM_001256268.2:c.799T=	NP_001243197.1:p.Ser267=
NM_032578.4:c.1681T= MANE Select	NP_115967.2:p.Ser561=