Canonical Allele Identifier: CA1917227365

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199369T= , CM000672.2:g.68199369T=	GRCh38
NC_000010.10:g.69959126T= , CM000672.1:g.69959126T=	GRCh37
NC_000010.9:g.69629132T=	NCBI36
NG_032118.1:g.98253T= , LRG_410:g.98253T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2462T=	ENSP00000346369.2:p.Val821=
ENST00000540630.6:c.3341T=	ENSP00000441668.3:p.Val1114=
ENST00000613327.5:c.3287T=	ENSP00000480757.2:p.Val1096=
ENST00000688812.1:c.*550T=	ENSP00000510658.1:n.*550T=
ENST00000690544.1:c.*2558T=	ENSP00000508989.1:n.*2558T=
ENST00000358913.10:c.3287T= MANE Select	ENSP00000351790.5:p.Val1096=
ENST00000354393.6:c.2462T=	ENSP00000346369.2:p.Val821=
ENST00000358913.9:c.3287T=	ENSP00000351790.5:p.Val1096=
ENST00000540630.5:c.3287T=	ENSP00000441668.2:p.Val1096=
ENST00000613327.4:c.2405T=	ENSP00000480757.1:p.Val802=
NM_001256267.1:c.3287T=	NP_001243196.1:p.Val1096=
NM_001256268.1:c.2405T=	NP_001243197.1:p.Val802=
NM_032578.3:c.3287T= , LRG_410t1:c.3287T=	NP_115967.2:p.Val1096=
NR_045662.3:n.2714T=
NR_045663.3:n.3416T=
XM_006718043.2:c.3341T=	XP_006718106.1:p.Val1114=
XM_011540292.1:c.3317T=	XP_011538594.1:p.Val1106=
XR_946029.1:n.1804-94A=
XM_017016833.1:c.3365T=	XP_016872322.1:p.Val1122=
XM_017016834.2:c.3287T=	XP_016872323.1:p.Val1096=
XM_024448236.1:c.2165T=	XP_024304004.1:p.Val722=
NR_045662.4:n.2824T=
NR_045663.4:n.3361T=
NM_001256267.2:c.3287T=	NP_001243196.1:p.Val1096=
NM_001256268.2:c.2405T=	NP_001243197.1:p.Val802=
NM_032578.4:c.3287T= MANE Select	NP_115967.2:p.Val1096=