Canonical Allele Identifier: CA1917227410

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199468A= , CM000672.2:g.68199468A=	GRCh38
NC_000010.10:g.69959225A= , CM000672.1:g.69959225A=	GRCh37
NC_000010.9:g.69629231A=	NCBI36
NG_032118.1:g.98352A= , LRG_410:g.98352A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2561A=	ENSP00000346369.2:p.His854=
ENST00000540630.6:c.3440A=	ENSP00000441668.3:p.His1147=
ENST00000613327.5:c.3386A=	ENSP00000480757.2:p.His1129=
ENST00000688812.1:c.*649A=	ENSP00000510658.1:n.*649A=
ENST00000690544.1:c.*2657A=	ENSP00000508989.1:n.*2657A=
ENST00000358913.10:c.3386A= MANE Select	ENSP00000351790.5:p.His1129=
ENST00000354393.6:c.2561A=	ENSP00000346369.2:p.His854=
ENST00000358913.9:c.3386A=	ENSP00000351790.5:p.His1129=
ENST00000540630.5:c.3386A=	ENSP00000441668.2:p.His1129=
ENST00000613327.4:c.2504A=	ENSP00000480757.1:p.His835=
NM_001256267.1:c.3386A=	NP_001243196.1:p.His1129=
NM_001256268.1:c.2504A=	NP_001243197.1:p.His835=
NM_032578.3:c.3386A= , LRG_410t1:c.3386A=	NP_115967.2:p.His1129=
NR_045662.3:n.2813A=
NR_045663.3:n.3515A=
XM_006718043.2:c.3440A=	XP_006718106.1:p.His1147=
XM_011540292.1:c.3416A=	XP_011538594.1:p.His1139=
XR_946029.1:n.1804-193T=
XM_017016833.1:c.3464A=	XP_016872322.1:p.His1155=
XM_017016834.2:c.3386A=	XP_016872323.1:p.His1129=
XM_024448236.1:c.2264A=	XP_024304004.1:p.His755=
NR_045662.4:n.2923A=
NR_045663.4:n.3460A=
NM_001256267.2:c.3386A=	NP_001243196.1:p.His1129=
NM_001256268.2:c.2504A=	NP_001243197.1:p.His835=
NM_032578.4:c.3386A= MANE Select	NP_115967.2:p.His1129=