Canonical Allele Identifier: CA1917215903

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166563A= , CM000672.2:g.68166563A=	GRCh38
NC_000010.10:g.69926320A= , CM000672.1:g.69926320A=	GRCh37
NC_000010.9:g.69596326A=	NCBI36
NG_032118.1:g.65447A= , LRG_410:g.65447A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1045A=	ENSP00000346369.2:p.Arg349=
ENST00000373675.4:c.1870A=	ENSP00000362779.4:p.Arg624=
ENST00000540630.6:c.1924A=	ENSP00000441668.3:p.Arg642=
ENST00000613327.5:c.1870A=	ENSP00000480757.2:p.Arg624=
ENST00000687572.1:c.748A=	ENSP00000510427.1:p.Arg250=
ENST00000688812.1:c.1846A=	ENSP00000510658.1:p.Arg616=
ENST00000690544.1:c.*1141A=	ENSP00000508989.1:n.*1141A=
ENST00000358913.10:c.1870A= MANE Select	ENSP00000351790.5:p.Arg624=
ENST00000354393.6:c.1045A=	ENSP00000346369.2:p.Arg349=
ENST00000358913.9:c.1870A=	ENSP00000351790.5:p.Arg624=
ENST00000540630.5:c.1870A=	ENSP00000441668.2:p.Arg624=
ENST00000613327.4:c.988A=	ENSP00000480757.1:p.Arg330=
NM_001256267.1:c.1870A=	NP_001243196.1:p.Arg624=
NM_001256268.1:c.988A=	NP_001243197.1:p.Arg330=
NM_032578.3:c.1870A= , LRG_410t1:c.1870A=	NP_115967.2:p.Arg624=
NR_045662.3:n.1297A=
NR_045663.3:n.2138A=
XM_006718043.2:c.1924A=	XP_006718106.1:p.Arg642=
XM_011540292.1:c.1900A=	XP_011538594.1:p.Arg634=
XM_017016833.1:c.1948A=	XP_016872322.1:p.Arg650=
XM_017016834.2:c.1870A=	XP_016872323.1:p.Arg624=
XM_024448236.1:c.748A=	XP_024304004.1:p.Arg250=
NR_045662.4:n.1407A=
NR_045663.4:n.2083A=
NM_001256267.2:c.1870A=	NP_001243196.1:p.Arg624=
NM_001256268.2:c.988A=	NP_001243197.1:p.Arg330=
NM_032578.4:c.1870A= MANE Select	NP_115967.2:p.Arg624=