Canonical Allele Identifier: CA1917215807

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166334C= , CM000672.2:g.68166334C=	GRCh38
NC_000010.10:g.69926091C= , CM000672.1:g.69926091C=	GRCh37
NC_000010.9:g.69596097C=	NCBI36
NG_032118.1:g.65218C= , LRG_410:g.65218C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.816C=	ENSP00000346369.2:p.Ala272=
ENST00000373675.4:c.1641C=	ENSP00000362779.4:p.Ala547=
ENST00000540630.6:c.1695C=	ENSP00000441668.3:p.Ala565=
ENST00000613327.5:c.1641C=	ENSP00000480757.2:p.Ala547=
ENST00000687572.1:c.519C=	ENSP00000510427.1:p.Ala173=
ENST00000687705.1:c.*1890C=	ENSP00000509639.1:n.*1890C=
ENST00000688812.1:c.1617C=	ENSP00000510658.1:p.Ala539=
ENST00000689002.1:n.693C=
ENST00000690544.1:c.*912C=	ENSP00000508989.1:n.*912C=
ENST00000358913.10:c.1641C= MANE Select	ENSP00000351790.5:p.Ala547=
ENST00000354393.6:c.816C=	ENSP00000346369.2:p.Ala272=
ENST00000358913.9:c.1641C=	ENSP00000351790.5:p.Ala547=
ENST00000540630.5:c.1641C=	ENSP00000441668.2:p.Ala547=
ENST00000613327.4:c.759C=	ENSP00000480757.1:p.Ala253=
NM_001256267.1:c.1641C=	NP_001243196.1:p.Ala547=
NM_001256268.1:c.759C=	NP_001243197.1:p.Ala253=
NM_032578.3:c.1641C= , LRG_410t1:c.1641C=	NP_115967.2:p.Ala547=
NR_045662.3:n.1068C=
NR_045663.3:n.1909C=
XM_006718043.2:c.1695C=	XP_006718106.1:p.Ala565=
XM_011540292.1:c.1671C=	XP_011538594.1:p.Ala557=
XM_017016833.1:c.1719C=	XP_016872322.1:p.Ala573=
XM_017016834.2:c.1641C=	XP_016872323.1:p.Ala547=
XM_024448236.1:c.519C=	XP_024304004.1:p.Ala173=
NR_045662.4:n.1178C=
NR_045663.4:n.1854C=
NM_001256267.2:c.1641C=	NP_001243196.1:p.Ala547=
NM_001256268.2:c.759C=	NP_001243197.1:p.Ala253=
NM_032578.4:c.1641C= MANE Select	NP_115967.2:p.Ala547=