Canonical Allele Identifier: CA1917225592

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68195531A= , CM000672.2:g.68195531A=	GRCh38
NC_000010.10:g.69955288A= , CM000672.1:g.69955288A=	GRCh37
NC_000010.9:g.69625294A=	NCBI36
NG_032118.1:g.94415A= , LRG_410:g.94415A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2332A=	ENSP00000346369.2:p.Arg778=
ENST00000540630.6:c.3211A=	ENSP00000441668.3:p.Arg1071=
ENST00000613327.5:c.3157A=	ENSP00000480757.2:p.Arg1053=
ENST00000688812.1:c.*420A=	ENSP00000510658.1:n.*420A=
ENST00000690544.1:c.*2428A=	ENSP00000508989.1:n.*2428A=
ENST00000358913.10:c.3157A= MANE Select	ENSP00000351790.5:p.Arg1053=
ENST00000354393.6:c.2332A=	ENSP00000346369.2:p.Arg778=
ENST00000358913.9:c.3157A=	ENSP00000351790.5:p.Arg1053=
ENST00000540630.5:c.3157A=	ENSP00000441668.2:p.Arg1053=
ENST00000613327.4:c.2275A=	ENSP00000480757.1:p.Arg759=
NM_001256267.1:c.3157A=	NP_001243196.1:p.Arg1053=
NM_001256268.1:c.2275A=	NP_001243197.1:p.Arg759=
NM_032578.3:c.3157A= , LRG_410t1:c.3157A=	NP_115967.2:p.Arg1053=
NR_045662.3:n.2584A=
NR_045663.3:n.3286A=
XM_006718043.2:c.3211A=	XP_006718106.1:p.Arg1071=
XM_011540292.1:c.3187A=	XP_011538594.1:p.Arg1063=
XM_017016833.1:c.3235A=	XP_016872322.1:p.Arg1079=
XM_017016834.2:c.3157A=	XP_016872323.1:p.Arg1053=
XM_024448236.1:c.2035A=	XP_024304004.1:p.Arg679=
NR_045662.4:n.2694A=
NR_045663.4:n.3231A=
NM_001256267.2:c.3157A=	NP_001243196.1:p.Arg1053=
NM_001256268.2:c.2275A=	NP_001243197.1:p.Arg759=
NM_032578.4:c.3157A= MANE Select	NP_115967.2:p.Arg1053=