Canonical Allele Identifier: CA1917232443

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68210428G= , CM000672.2:g.68210428G=	GRCh38
NC_000010.10:g.69970185G= , CM000672.1:g.69970185G=	GRCh37
NC_000010.9:g.69640191G=	NCBI36
NG_032118.1:g.109312G= , LRG_410:g.109312G=

Transcript Alleles

HGVS	Amino-acid Change
NM_032578.4:c.3936G= MANE Select	NP_115967.2:p.Arg1312=
ENST00000358913.10:c.3936G= MANE Select	ENSP00000351790.5:p.Arg1312=
NM_001256267.1:c.3936G=	NP_001243196.1:p.Arg1312=
NM_001256267.2:c.3936G=	NP_001243196.1:p.Arg1312=
NM_001256268.1:c.3054G=	NP_001243197.1:p.Arg1018=
NM_001256268.2:c.3054G=	NP_001243197.1:p.Arg1018=
NM_032578.3:c.3936G= , LRG_410t1:c.3936G=	NP_115967.2:p.Arg1312=
NR_045662.3:n.3363G=
NR_045662.4:n.3473G=
NR_045663.3:n.4065G=
NR_045663.4:n.4010G=
ENST00000354393.6:c.3111G=	ENSP00000346369.2:p.Arg1037=
ENST00000354393.7:c.3111G=	ENSP00000346369.2:p.Arg1037=
ENST00000358913.9:c.3936G=	ENSP00000351790.5:p.Arg1312=
ENST00000540630.5:c.3936G=	ENSP00000441668.2:p.Arg1312=
ENST00000540630.6:c.3990G=	ENSP00000441668.3:p.Arg1330=
ENST00000613327.4:c.3054G=	ENSP00000480757.1:p.Arg1018=
ENST00000613327.5:c.3936G=	ENSP00000480757.2:p.Arg1312=
ENST00000688812.1:c.*1199G=	ENSP00000510658.1:n.*1199G=
ENST00000690544.1:c.*3207G=	ENSP00000508989.1:n.*3207G=
XM_006718043.2:c.3990G=	XP_006718106.1:p.Arg1330=
XM_011540292.1:c.3966G=	XP_011538594.1:p.Arg1322=
XM_017016833.1:c.4014G=	XP_016872322.1:p.Arg1338=
XM_017016834.2:c.3936G=	XP_016872323.1:p.Arg1312=
XM_024448236.1:c.2814G=	XP_024304004.1:p.Arg938=
XR_946029.1:n.1574+4860C=