Canonical Allele Identifier: CA1917215899

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166553C= , CM000672.2:g.68166553C=	GRCh38
NC_000010.10:g.69926310C= , CM000672.1:g.69926310C=	GRCh37
NC_000010.9:g.69596316C=	NCBI36
NG_032118.1:g.65437C= , LRG_410:g.65437C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1035C=	ENSP00000346369.2:p.Thr345=
ENST00000373675.4:c.1860C=	ENSP00000362779.4:p.Thr620=
ENST00000540630.6:c.1914C=	ENSP00000441668.3:p.Thr638=
ENST00000613327.5:c.1860C=	ENSP00000480757.2:p.Thr620=
ENST00000687572.1:c.738C=	ENSP00000510427.1:p.Thr246=
ENST00000688812.1:c.1836C=	ENSP00000510658.1:p.Thr612=
ENST00000690544.1:c.*1131C=	ENSP00000508989.1:n.*1131C=
ENST00000358913.10:c.1860C= MANE Select	ENSP00000351790.5:p.Thr620=
ENST00000354393.6:c.1035C=	ENSP00000346369.2:p.Thr345=
ENST00000358913.9:c.1860C=	ENSP00000351790.5:p.Thr620=
ENST00000540630.5:c.1860C=	ENSP00000441668.2:p.Thr620=
ENST00000613327.4:c.978C=	ENSP00000480757.1:p.Thr326=
NM_001256267.1:c.1860C=	NP_001243196.1:p.Thr620=
NM_001256268.1:c.978C=	NP_001243197.1:p.Thr326=
NM_032578.3:c.1860C= , LRG_410t1:c.1860C=	NP_115967.2:p.Thr620=
NR_045662.3:n.1287C=
NR_045663.3:n.2128C=
XM_006718043.2:c.1914C=	XP_006718106.1:p.Thr638=
XM_011540292.1:c.1890C=	XP_011538594.1:p.Thr630=
XM_017016833.1:c.1938C=	XP_016872322.1:p.Thr646=
XM_017016834.2:c.1860C=	XP_016872323.1:p.Thr620=
XM_024448236.1:c.738C=	XP_024304004.1:p.Thr246=
NR_045662.4:n.1397C=
NR_045663.4:n.2073C=
NM_001256267.2:c.1860C=	NP_001243196.1:p.Thr620=
NM_001256268.2:c.978C=	NP_001243197.1:p.Thr326=
NM_032578.4:c.1860C= MANE Select	NP_115967.2:p.Thr620=