Canonical Allele Identifier: CA1917215827

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166379A= , CM000672.2:g.68166379A=	GRCh38
NC_000010.10:g.69926136A= , CM000672.1:g.69926136A=	GRCh37
NC_000010.9:g.69596142A=	NCBI36
NG_032118.1:g.65263A= , LRG_410:g.65263A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.861A=	ENSP00000346369.2:p.Pro287=
ENST00000373675.4:c.1686A=	ENSP00000362779.4:p.Pro562=
ENST00000540630.6:c.1740A=	ENSP00000441668.3:p.Pro580=
ENST00000613327.5:c.1686A=	ENSP00000480757.2:p.Pro562=
ENST00000687572.1:c.564A=	ENSP00000510427.1:p.Pro188=
ENST00000688812.1:c.1662A=	ENSP00000510658.1:p.Pro554=
ENST00000689002.1:n.738A=
ENST00000690544.1:c.*957A=	ENSP00000508989.1:n.*957A=
ENST00000358913.10:c.1686A= MANE Select	ENSP00000351790.5:p.Pro562=
ENST00000354393.6:c.861A=	ENSP00000346369.2:p.Pro287=
ENST00000358913.9:c.1686A=	ENSP00000351790.5:p.Pro562=
ENST00000540630.5:c.1686A=	ENSP00000441668.2:p.Pro562=
ENST00000613327.4:c.804A=	ENSP00000480757.1:p.Pro268=
NM_001256267.1:c.1686A=	NP_001243196.1:p.Pro562=
NM_001256268.1:c.804A=	NP_001243197.1:p.Pro268=
NM_032578.3:c.1686A= , LRG_410t1:c.1686A=	NP_115967.2:p.Pro562=
NR_045662.3:n.1113A=
NR_045663.3:n.1954A=
XM_006718043.2:c.1740A=	XP_006718106.1:p.Pro580=
XM_011540292.1:c.1716A=	XP_011538594.1:p.Pro572=
XM_017016833.1:c.1764A=	XP_016872322.1:p.Pro588=
XM_017016834.2:c.1686A=	XP_016872323.1:p.Pro562=
XM_024448236.1:c.564A=	XP_024304004.1:p.Pro188=
NR_045662.4:n.1223A=
NR_045663.4:n.1899A=
NM_001256267.2:c.1686A=	NP_001243196.1:p.Pro562=
NM_001256268.2:c.804A=	NP_001243197.1:p.Pro268=
NM_032578.4:c.1686A= MANE Select	NP_115967.2:p.Pro562=