Canonical Allele Identifier: CA1917215921

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166604A= , CM000672.2:g.68166604A=	GRCh38
NC_000010.10:g.69926361A= , CM000672.1:g.69926361A=	GRCh37
NC_000010.9:g.69596367A=	NCBI36
NG_032118.1:g.65488A= , LRG_410:g.65488A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1086A=	ENSP00000346369.2:p.Thr362=
ENST00000373675.4:c.1911A=	ENSP00000362779.4:p.Thr637=
ENST00000540630.6:c.1965A=	ENSP00000441668.3:p.Thr655=
ENST00000613327.5:c.1911A=	ENSP00000480757.2:p.Thr637=
ENST00000687572.1:c.789A=	ENSP00000510427.1:p.Thr263=
ENST00000688812.1:c.1887A=	ENSP00000510658.1:p.Thr629=
ENST00000690544.1:c.*1182A=	ENSP00000508989.1:n.*1182A=
ENST00000358913.10:c.1911A= MANE Select	ENSP00000351790.5:p.Thr637=
ENST00000354393.6:c.1086A=	ENSP00000346369.2:p.Thr362=
ENST00000358913.9:c.1911A=	ENSP00000351790.5:p.Thr637=
ENST00000540630.5:c.1911A=	ENSP00000441668.2:p.Thr637=
ENST00000613327.4:c.1029A=	ENSP00000480757.1:p.Thr343=
NM_001256267.1:c.1911A=	NP_001243196.1:p.Thr637=
NM_001256268.1:c.1029A=	NP_001243197.1:p.Thr343=
NM_032578.3:c.1911A= , LRG_410t1:c.1911A=	NP_115967.2:p.Thr637=
NR_045662.3:n.1338A=
NR_045663.3:n.2179A=
XM_006718043.2:c.1965A=	XP_006718106.1:p.Thr655=
XM_011540292.1:c.1941A=	XP_011538594.1:p.Thr647=
XM_017016833.1:c.1989A=	XP_016872322.1:p.Thr663=
XM_017016834.2:c.1911A=	XP_016872323.1:p.Thr637=
XM_024448236.1:c.789A=	XP_024304004.1:p.Thr263=
NR_045662.4:n.1448A=
NR_045663.4:n.2124A=
NM_001256267.2:c.1911A=	NP_001243196.1:p.Thr637=
NM_001256268.2:c.1029A=	NP_001243197.1:p.Thr343=
NM_032578.4:c.1911A= MANE Select	NP_115967.2:p.Thr637=