Canonical Allele Identifier: CA1917226437

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68197363G= , CM000672.2:g.68197363G=	GRCh38
NC_000010.10:g.69957120G= , CM000672.1:g.69957120G=	GRCh37
NC_000010.9:g.69627126G=	NCBI36
NG_032118.1:g.96247G= , LRG_410:g.96247G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2345G=	ENSP00000346369.2:p.Arg782=
ENST00000540630.6:c.3224G=	ENSP00000441668.3:p.Arg1075=
ENST00000613327.5:c.3170G=	ENSP00000480757.2:p.Arg1057=
ENST00000688812.1:c.*433G=	ENSP00000510658.1:n.*433G=
ENST00000690544.1:c.*2441G=	ENSP00000508989.1:n.*2441G=
ENST00000358913.10:c.3170G= MANE Select	ENSP00000351790.5:p.Arg1057=
ENST00000354393.6:c.2345G=	ENSP00000346369.2:p.Arg782=
ENST00000358913.9:c.3170G=	ENSP00000351790.5:p.Arg1057=
ENST00000540630.5:c.3170G=	ENSP00000441668.2:p.Arg1057=
ENST00000613327.4:c.2288G=	ENSP00000480757.1:p.Arg763=
NM_001256267.1:c.3170G=	NP_001243196.1:p.Arg1057=
NM_001256268.1:c.2288G=	NP_001243197.1:p.Arg763=
NM_032578.3:c.3170G= , LRG_410t1:c.3170G=	NP_115967.2:p.Arg1057=
NR_045662.3:n.2597G=
NR_045663.3:n.3299G=
XM_006718043.2:c.3224G=	XP_006718106.1:p.Arg1075=
XM_011540292.1:c.3200G=	XP_011538594.1:p.Arg1067=
XM_017016833.1:c.3248G=	XP_016872322.1:p.Arg1083=
XM_017016834.2:c.3170G=	XP_016872323.1:p.Arg1057=
XM_024448236.1:c.2048G=	XP_024304004.1:p.Arg683=
NR_045662.4:n.2707G=
NR_045663.4:n.3244G=
NM_001256267.2:c.3170G=	NP_001243196.1:p.Arg1057=
NM_001256268.2:c.2288G=	NP_001243197.1:p.Arg763=
NM_032578.4:c.3170G= MANE Select	NP_115967.2:p.Arg1057=