Canonical Allele Identifier: CA1917215614

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68165814G= , CM000672.2:g.68165814G=	GRCh38
NC_000010.10:g.69925571G= , CM000672.1:g.69925571G=	GRCh37
NC_000010.9:g.69595577G=	NCBI36
NG_032118.1:g.64698G= , LRG_410:g.64698G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.771G=	ENSP00000346369.2:p.Val257=
ENST00000373675.4:c.1596G=	ENSP00000362779.4:p.Val532=
ENST00000540630.6:c.1650G=	ENSP00000441668.3:p.Val550=
ENST00000613327.5:c.1596G=	ENSP00000480757.2:p.Val532=
ENST00000687572.1:c.474G=	ENSP00000510427.1:p.Val158=
ENST00000687705.1:c.*1845G=	ENSP00000509639.1:n.*1845G=
ENST00000688812.1:c.1572G=	ENSP00000510658.1:p.Val524=
ENST00000689002.1:n.648G=
ENST00000690544.1:c.*867G=	ENSP00000508989.1:n.*867G=
ENST00000358913.10:c.1596G= MANE Select	ENSP00000351790.5:p.Val532=
ENST00000354393.6:c.771G=	ENSP00000346369.2:p.Val257=
ENST00000358913.9:c.1596G=	ENSP00000351790.5:p.Val532=
ENST00000540630.5:c.1596G=	ENSP00000441668.2:p.Val532=
ENST00000613327.4:c.714G=	ENSP00000480757.1:p.Val238=
NM_001256267.1:c.1596G=	NP_001243196.1:p.Val532=
NM_001256268.1:c.714G=	NP_001243197.1:p.Val238=
NM_032578.3:c.1596G= , LRG_410t1:c.1596G=	NP_115967.2:p.Val532=
NR_045662.3:n.1023G=
NR_045663.3:n.1864G=
XM_006718043.2:c.1650G=	XP_006718106.1:p.Val550=
XM_011540292.1:c.1626G=	XP_011538594.1:p.Val542=
XM_017016833.1:c.1674G=	XP_016872322.1:p.Val558=
XM_017016834.2:c.1596G=	XP_016872323.1:p.Val532=
XM_024448236.1:c.474G=	XP_024304004.1:p.Val158=
NR_045662.4:n.1133G=
NR_045663.4:n.1809G=
NM_001256267.2:c.1596G=	NP_001243196.1:p.Val532=
NM_001256268.2:c.714G=	NP_001243197.1:p.Val238=
NM_032578.4:c.1596G= MANE Select	NP_115967.2:p.Val532=