Canonical Allele Identifier: CA1917227375

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199388G= , CM000672.2:g.68199388G=	GRCh38
NC_000010.10:g.69959145G= , CM000672.1:g.69959145G=	GRCh37
NC_000010.9:g.69629151G=	NCBI36
NG_032118.1:g.98272G= , LRG_410:g.98272G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2481G=	ENSP00000346369.2:p.Pro827=
ENST00000540630.6:c.3360G=	ENSP00000441668.3:p.Pro1120=
ENST00000613327.5:c.3306G=	ENSP00000480757.2:p.Pro1102=
ENST00000688812.1:c.*569G=	ENSP00000510658.1:n.*569G=
ENST00000690544.1:c.*2577G=	ENSP00000508989.1:n.*2577G=
ENST00000358913.10:c.3306G= MANE Select	ENSP00000351790.5:p.Pro1102=
ENST00000354393.6:c.2481G=	ENSP00000346369.2:p.Pro827=
ENST00000358913.9:c.3306G=	ENSP00000351790.5:p.Pro1102=
ENST00000540630.5:c.3306G=	ENSP00000441668.2:p.Pro1102=
ENST00000613327.4:c.2424G=	ENSP00000480757.1:p.Pro808=
NM_001256267.1:c.3306G=	NP_001243196.1:p.Pro1102=
NM_001256268.1:c.2424G=	NP_001243197.1:p.Pro808=
NM_032578.3:c.3306G= , LRG_410t1:c.3306G=	NP_115967.2:p.Pro1102=
NR_045662.3:n.2733G=
NR_045663.3:n.3435G=
XM_006718043.2:c.3360G=	XP_006718106.1:p.Pro1120=
XM_011540292.1:c.3336G=	XP_011538594.1:p.Pro1112=
XR_946029.1:n.1804-113C=
XM_017016833.1:c.3384G=	XP_016872322.1:p.Pro1128=
XM_017016834.2:c.3306G=	XP_016872323.1:p.Pro1102=
XM_024448236.1:c.2184G=	XP_024304004.1:p.Pro728=
NR_045662.4:n.2843G=
NR_045663.4:n.3380G=
NM_001256267.2:c.3306G=	NP_001243196.1:p.Pro1102=
NM_001256268.2:c.2424G=	NP_001243197.1:p.Pro808=
NM_032578.4:c.3306G= MANE Select	NP_115967.2:p.Pro1102=