Canonical Allele Identifier: CA1917232512

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68210574G= , CM000672.2:g.68210574G=	GRCh38
NC_000010.10:g.69970331G= , CM000672.1:g.69970331G=	GRCh37
NC_000010.9:g.69640337G=	NCBI36
NG_032118.1:g.109458G= , LRG_410:g.109458G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.*119G=	ENSP00000346369.2:n.*119G=
ENST00000540630.6:c.*119G=	ENSP00000441668.3:n.*119G=
ENST00000613327.5:c.*119G=	ENSP00000480757.2:n.*119G=
ENST00000688812.1:c.*1345G=	ENSP00000510658.1:n.*1345G=
ENST00000690544.1:c.*3353G=	ENSP00000508989.1:n.*3353G=
ENST00000358913.10:c.*119G= MANE Select	ENSP00000351790.5:n.*119G=
ENST00000354393.6:c.*119G=	ENSP00000346369.2:n.*119G=
ENST00000358913.9:c.*119G=	ENSP00000351790.5:n.*119G=
ENST00000540630.5:c.*119G=	ENSP00000441668.2:n.*119G=
ENST00000613327.4:c.*119G=	ENSP00000480757.1:n.*119G=
NM_001256267.1:c.*119G=	NP_001243196.1:n.*119G=
NM_001256268.1:c.*119G=	NP_001243197.1:n.*119G=
NM_032578.3:c.*119G= , LRG_410t1:c.*119G=	NP_115967.2:n.*119G=
NR_045662.3:n.3509G=
NR_045663.3:n.4211G=
XM_006718043.2:c.*119G=	XP_006718106.1:n.*119G=
XM_011540292.1:c.*119G=	XP_011538594.1:n.*119G=
XR_946029.1:n.1574+4714C=
XM_017016833.1:c.*119G=	XP_016872322.1:n.*119G=
XM_017016834.2:c.*119G=	XP_016872323.1:n.*119G=
XM_024448236.1:c.*119G=	XP_024304004.1:n.*119G=
NR_045662.4:n.3619G=
NR_045663.4:n.4156G=
NM_001256267.2:c.*119G=	NP_001243196.1:n.*119G=
NM_001256268.2:c.*119G=	NP_001243197.1:n.*119G=
NM_032578.4:c.*119G= MANE Select	NP_115967.2:n.*119G=