Canonical Allele Identifier: CA1917225576

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68195498C= , CM000672.2:g.68195498C=	GRCh38
NC_000010.10:g.69955255C= , CM000672.1:g.69955255C=	GRCh37
NC_000010.9:g.69625261C=	NCBI36
NG_032118.1:g.94382C= , LRG_410:g.94382C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2299C=	ENSP00000346369.2:p.Arg767=
ENST00000540630.6:c.3178C=	ENSP00000441668.3:p.Arg1060=
ENST00000613327.5:c.3124C=	ENSP00000480757.2:p.Arg1042=
ENST00000688812.1:c.*387C=	ENSP00000510658.1:n.*387C=
ENST00000690544.1:c.*2395C=	ENSP00000508989.1:n.*2395C=
ENST00000358913.10:c.3124C= MANE Select	ENSP00000351790.5:p.Arg1042=
ENST00000354393.6:c.2299C=	ENSP00000346369.2:p.Arg767=
ENST00000358913.9:c.3124C=	ENSP00000351790.5:p.Arg1042=
ENST00000540630.5:c.3124C=	ENSP00000441668.2:p.Arg1042=
ENST00000613327.4:c.2242C=	ENSP00000480757.1:p.Arg748=
NM_001256267.1:c.3124C=	NP_001243196.1:p.Arg1042=
NM_001256268.1:c.2242C=	NP_001243197.1:p.Arg748=
NM_032578.3:c.3124C= , LRG_410t1:c.3124C=	NP_115967.2:p.Arg1042=
NR_045662.3:n.2551C=
NR_045663.3:n.3253C=
XM_006718043.2:c.3178C=	XP_006718106.1:p.Arg1060=
XM_011540292.1:c.3154C=	XP_011538594.1:p.Arg1052=
XM_017016833.1:c.3202C=	XP_016872322.1:p.Arg1068=
XM_017016834.2:c.3124C=	XP_016872323.1:p.Arg1042=
XM_024448236.1:c.2002C=	XP_024304004.1:p.Arg668=
NR_045662.4:n.2661C=
NR_045663.4:n.3198C=
NM_001256267.2:c.3124C=	NP_001243196.1:p.Arg1042=
NM_001256268.2:c.2242C=	NP_001243197.1:p.Arg748=
NM_032578.4:c.3124C= MANE Select	NP_115967.2:p.Arg1042=