Canonical Allele Identifier: CA1917215942

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166645C= , CM000672.2:g.68166645C=	GRCh38
NC_000010.10:g.69926402C= , CM000672.1:g.69926402C=	GRCh37
NC_000010.9:g.69596408C=	NCBI36
NG_032118.1:g.65529C= , LRG_410:g.65529C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1127C=	ENSP00000346369.2:p.Pro376=
ENST00000373675.4:c.1952C=	ENSP00000362779.4:p.Pro651=
ENST00000540630.6:c.2006C=	ENSP00000441668.3:p.Pro669=
ENST00000613327.5:c.1952C=	ENSP00000480757.2:p.Pro651=
ENST00000687572.1:c.830C=	ENSP00000510427.1:p.Pro277=
ENST00000688812.1:c.1928C=	ENSP00000510658.1:p.Pro643=
ENST00000690544.1:c.*1223C=	ENSP00000508989.1:n.*1223C=
ENST00000358913.10:c.1952C= MANE Select	ENSP00000351790.5:p.Pro651=
ENST00000354393.6:c.1127C=	ENSP00000346369.2:p.Pro376=
ENST00000358913.9:c.1952C=	ENSP00000351790.5:p.Pro651=
ENST00000540630.5:c.1952C=	ENSP00000441668.2:p.Pro651=
ENST00000613327.4:c.1070C=	ENSP00000480757.1:p.Pro357=
NM_001256267.1:c.1952C=	NP_001243196.1:p.Pro651=
NM_001256268.1:c.1070C=	NP_001243197.1:p.Pro357=
NM_032578.3:c.1952C= , LRG_410t1:c.1952C=	NP_115967.2:p.Pro651=
NR_045662.3:n.1379C=
NR_045663.3:n.2220C=
XM_006718043.2:c.2006C=	XP_006718106.1:p.Pro669=
XM_011540292.1:c.1982C=	XP_011538594.1:p.Pro661=
XM_017016833.1:c.2030C=	XP_016872322.1:p.Pro677=
XM_017016834.2:c.1952C=	XP_016872323.1:p.Pro651=
XM_024448236.1:c.830C=	XP_024304004.1:p.Pro277=
NR_045662.4:n.1489C=
NR_045663.4:n.2165C=
NM_001256267.2:c.1952C=	NP_001243196.1:p.Pro651=
NM_001256268.2:c.1070C=	NP_001243197.1:p.Pro357=
NM_032578.4:c.1952C= MANE Select	NP_115967.2:p.Pro651=