Canonical Allele Identifier: CA1917215932

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166630T= , CM000672.2:g.68166630T=	GRCh38
NC_000010.10:g.69926387T= , CM000672.1:g.69926387T=	GRCh37
NC_000010.9:g.69596393T=	NCBI36
NG_032118.1:g.65514T= , LRG_410:g.65514T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1112T=	ENSP00000346369.2:p.Val371=
ENST00000373675.4:c.1937T=	ENSP00000362779.4:p.Val646=
ENST00000540630.6:c.1991T=	ENSP00000441668.3:p.Val664=
ENST00000613327.5:c.1937T=	ENSP00000480757.2:p.Val646=
ENST00000687572.1:c.815T=	ENSP00000510427.1:p.Val272=
ENST00000688812.1:c.1913T=	ENSP00000510658.1:p.Val638=
ENST00000690544.1:c.*1208T=	ENSP00000508989.1:n.*1208T=
ENST00000358913.10:c.1937T= MANE Select	ENSP00000351790.5:p.Val646=
ENST00000354393.6:c.1112T=	ENSP00000346369.2:p.Val371=
ENST00000358913.9:c.1937T=	ENSP00000351790.5:p.Val646=
ENST00000540630.5:c.1937T=	ENSP00000441668.2:p.Val646=
ENST00000613327.4:c.1055T=	ENSP00000480757.1:p.Val352=
NM_001256267.1:c.1937T=	NP_001243196.1:p.Val646=
NM_001256268.1:c.1055T=	NP_001243197.1:p.Val352=
NM_032578.3:c.1937T= , LRG_410t1:c.1937T=	NP_115967.2:p.Val646=
NR_045662.3:n.1364T=
NR_045663.3:n.2205T=
XM_006718043.2:c.1991T=	XP_006718106.1:p.Val664=
XM_011540292.1:c.1967T=	XP_011538594.1:p.Val656=
XM_017016833.1:c.2015T=	XP_016872322.1:p.Val672=
XM_017016834.2:c.1937T=	XP_016872323.1:p.Val646=
XM_024448236.1:c.815T=	XP_024304004.1:p.Val272=
NR_045662.4:n.1474T=
NR_045663.4:n.2150T=
NM_001256267.2:c.1937T=	NP_001243196.1:p.Val646=
NM_001256268.2:c.1055T=	NP_001243197.1:p.Val352=
NM_032578.4:c.1937T= MANE Select	NP_115967.2:p.Val646=