Canonical Allele Identifier: CA1917215576

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68165717T= , CM000672.2:g.68165717T=	GRCh38
NC_000010.10:g.69925474T= , CM000672.1:g.69925474T=	GRCh37
NC_000010.9:g.69595480T=	NCBI36
NG_032118.1:g.64601T= , LRG_410:g.64601T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.674T=	ENSP00000346369.2:p.Leu225=
ENST00000373675.4:c.1499T=	ENSP00000362779.4:p.Leu500=
ENST00000540630.6:c.1553T=	ENSP00000441668.3:p.Leu518=
ENST00000613327.5:c.1499T=	ENSP00000480757.2:p.Leu500=
ENST00000687572.1:c.377T=	ENSP00000510427.1:p.Leu126=
ENST00000687705.1:c.*1748T=	ENSP00000509639.1:n.*1748T=
ENST00000688812.1:c.1475T=	ENSP00000510658.1:p.Leu492=
ENST00000689002.1:n.551T=
ENST00000690544.1:c.*770T=	ENSP00000508989.1:n.*770T=
ENST00000358913.10:c.1499T= MANE Select	ENSP00000351790.5:p.Leu500=
ENST00000354393.6:c.674T=	ENSP00000346369.2:p.Leu225=
ENST00000358913.9:c.1499T=	ENSP00000351790.5:p.Leu500=
ENST00000540630.5:c.1499T=	ENSP00000441668.2:p.Leu500=
ENST00000613327.4:c.617T=	ENSP00000480757.1:p.Leu206=
NM_001256267.1:c.1499T=	NP_001243196.1:p.Leu500=
NM_001256268.1:c.617T=	NP_001243197.1:p.Leu206=
NM_032578.3:c.1499T= , LRG_410t1:c.1499T=	NP_115967.2:p.Leu500=
NR_045662.3:n.926T=
NR_045663.3:n.1767T=
XM_006718043.2:c.1553T=	XP_006718106.1:p.Leu518=
XM_011540292.1:c.1529T=	XP_011538594.1:p.Leu510=
XM_017016833.1:c.1577T=	XP_016872322.1:p.Leu526=
XM_017016834.2:c.1499T=	XP_016872323.1:p.Leu500=
XM_024448236.1:c.377T=	XP_024304004.1:p.Leu126=
NR_045662.4:n.1036T=
NR_045663.4:n.1712T=
NM_001256267.2:c.1499T=	NP_001243196.1:p.Leu500=
NM_001256268.2:c.617T=	NP_001243197.1:p.Leu206=
NM_032578.4:c.1499T= MANE Select	NP_115967.2:p.Leu500=