Canonical Allele Identifier: CA1917215792

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166272G= , CM000672.2:g.68166272G=	GRCh38
NC_000010.10:g.69926029G= , CM000672.1:g.69926029G=	GRCh37
NC_000010.9:g.69596035G=	NCBI36
NG_032118.1:g.65156G= , LRG_410:g.65156G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.776-22G=	ENSP00000346369.2:n.776-22G=
ENST00000373675.4:c.1601-22G=	ENSP00000362779.4:n.1601-22G=
ENST00000540630.6:c.1655-22G=	ENSP00000441668.3:n.1655-22G=
ENST00000613327.5:c.1601-22G=	ENSP00000480757.2:n.1601-22G=
ENST00000687572.1:c.479-22G=	ENSP00000510427.1:n.479-22G=
ENST00000687705.1:c.*1850-22G=	ENSP00000509639.1:n.*1850-22G=
ENST00000688812.1:c.1577-22G=	ENSP00000510658.1:n.1577-22G=
ENST00000689002.1:n.653-22G=
ENST00000690544.1:c.*872-22G=	ENSP00000508989.1:n.*872-22G=
ENST00000358913.10:c.1601-22G= MANE Select	ENSP00000351790.5:n.1601-22G=
ENST00000354393.6:c.776-22G=	ENSP00000346369.2:n.776-22G=
ENST00000358913.9:c.1601-22G=	ENSP00000351790.5:n.1601-22G=
ENST00000540630.5:c.1601-22G=	ENSP00000441668.2:n.1601-22G=
ENST00000613327.4:c.719-22G=	ENSP00000480757.1:n.719-22G=
NM_001256267.1:c.1601-22G=	NP_001243196.1:n.1601-22G=
NM_001256268.1:c.719-22G=	NP_001243197.1:n.719-22G=
NM_032578.3:c.1601-22G= , LRG_410t1:c.1601-22G=	NP_115967.2:n.1601-22G=
NR_045662.3:n.1028-22G=
NR_045663.3:n.1869-22G=
XM_006718043.2:c.1655-22G=	XP_006718106.1:n.1655-22G=
XM_011540292.1:c.1631-22G=	XP_011538594.1:n.1631-22G=
XM_017016833.1:c.1679-22G=	XP_016872322.1:n.1679-22G=
XM_017016834.2:c.1601-22G=	XP_016872323.1:n.1601-22G=
XM_024448236.1:c.479-22G=	XP_024304004.1:n.479-22G=
NR_045662.4:n.1138-22G=
NR_045663.4:n.1814-22G=
NM_001256267.2:c.1601-22G=	NP_001243196.1:n.1601-22G=
NM_001256268.2:c.719-22G=	NP_001243197.1:n.719-22G=
NM_032578.4:c.1601-22G= MANE Select	NP_115967.2:n.1601-22G=