Canonical Allele Identifier: CA1917215784

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166258T= , CM000672.2:g.68166258T=	GRCh38
NC_000010.10:g.69926015T= , CM000672.1:g.69926015T=	GRCh37
NC_000010.9:g.69596021T=	NCBI36
NG_032118.1:g.65142T= , LRG_410:g.65142T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.776-36T=	ENSP00000346369.2:n.776-36T=
ENST00000373675.4:c.1601-36T=	ENSP00000362779.4:n.1601-36T=
ENST00000540630.6:c.1655-36T=	ENSP00000441668.3:n.1655-36T=
ENST00000613327.5:c.1601-36T=	ENSP00000480757.2:n.1601-36T=
ENST00000687572.1:c.479-36T=	ENSP00000510427.1:n.479-36T=
ENST00000687705.1:c.*1850-36T=	ENSP00000509639.1:n.*1850-36T=
ENST00000688812.1:c.1577-36T=	ENSP00000510658.1:n.1577-36T=
ENST00000689002.1:n.653-36T=
ENST00000690544.1:c.*872-36T=	ENSP00000508989.1:n.*872-36T=
ENST00000358913.10:c.1601-36T= MANE Select	ENSP00000351790.5:n.1601-36T=
ENST00000354393.6:c.776-36T=	ENSP00000346369.2:n.776-36T=
ENST00000358913.9:c.1601-36T=	ENSP00000351790.5:n.1601-36T=
ENST00000540630.5:c.1601-36T=	ENSP00000441668.2:n.1601-36T=
ENST00000613327.4:c.719-36T=	ENSP00000480757.1:n.719-36T=
NM_001256267.1:c.1601-36T=	NP_001243196.1:n.1601-36T=
NM_001256268.1:c.719-36T=	NP_001243197.1:n.719-36T=
NM_032578.3:c.1601-36T= , LRG_410t1:c.1601-36T=	NP_115967.2:n.1601-36T=
NR_045662.3:n.1028-36T=
NR_045663.3:n.1869-36T=
XM_006718043.2:c.1655-36T=	XP_006718106.1:n.1655-36T=
XM_011540292.1:c.1631-36T=	XP_011538594.1:n.1631-36T=
XM_017016833.1:c.1679-36T=	XP_016872322.1:n.1679-36T=
XM_017016834.2:c.1601-36T=	XP_016872323.1:n.1601-36T=
XM_024448236.1:c.479-36T=	XP_024304004.1:n.479-36T=
NR_045662.4:n.1138-36T=
NR_045663.4:n.1814-36T=
NM_001256267.2:c.1601-36T=	NP_001243196.1:n.1601-36T=
NM_001256268.2:c.719-36T=	NP_001243197.1:n.719-36T=
NM_032578.4:c.1601-36T= MANE Select	NP_115967.2:n.1601-36T=