Canonical Allele Identifier: CA1917215806

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166317G= , CM000672.2:g.68166317G=	GRCh38
NC_000010.10:g.69926074G= , CM000672.1:g.69926074G=	GRCh37
NC_000010.9:g.69596080G=	NCBI36
NG_032118.1:g.65201G= , LRG_410:g.65201G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.799G=	ENSP00000346369.2:p.Gly267=
ENST00000373675.4:c.1624G=	ENSP00000362779.4:p.Gly542=
ENST00000540630.6:c.1678G=	ENSP00000441668.3:p.Gly560=
ENST00000613327.5:c.1624G=	ENSP00000480757.2:p.Gly542=
ENST00000687572.1:c.502G=	ENSP00000510427.1:p.Gly168=
ENST00000687705.1:c.*1873G=	ENSP00000509639.1:n.*1873G=
ENST00000688812.1:c.1600G=	ENSP00000510658.1:p.Gly534=
ENST00000689002.1:n.676G=
ENST00000690544.1:c.*895G=	ENSP00000508989.1:n.*895G=
ENST00000358913.10:c.1624G= MANE Select	ENSP00000351790.5:p.Gly542=
ENST00000354393.6:c.799G=	ENSP00000346369.2:p.Gly267=
ENST00000358913.9:c.1624G=	ENSP00000351790.5:p.Gly542=
ENST00000540630.5:c.1624G=	ENSP00000441668.2:p.Gly542=
ENST00000613327.4:c.742G=	ENSP00000480757.1:p.Gly248=
NM_001256267.1:c.1624G=	NP_001243196.1:p.Gly542=
NM_001256268.1:c.742G=	NP_001243197.1:p.Gly248=
NM_032578.3:c.1624G= , LRG_410t1:c.1624G=	NP_115967.2:p.Gly542=
NR_045662.3:n.1051G=
NR_045663.3:n.1892G=
XM_006718043.2:c.1678G=	XP_006718106.1:p.Gly560=
XM_011540292.1:c.1654G=	XP_011538594.1:p.Gly552=
XM_017016833.1:c.1702G=	XP_016872322.1:p.Gly568=
XM_017016834.2:c.1624G=	XP_016872323.1:p.Gly542=
XM_024448236.1:c.502G=	XP_024304004.1:p.Gly168=
NR_045662.4:n.1161G=
NR_045663.4:n.1837G=
NM_001256267.2:c.1624G=	NP_001243196.1:p.Gly542=
NM_001256268.2:c.742G=	NP_001243197.1:p.Gly248=
NM_032578.4:c.1624G= MANE Select	NP_115967.2:p.Gly542=