Canonical Allele Identifier: CA1917227418

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199490C= , CM000672.2:g.68199490C=	GRCh38
NC_000010.10:g.69959247C= , CM000672.1:g.69959247C=	GRCh37
NC_000010.9:g.69629253C=	NCBI36
NG_032118.1:g.98374C= , LRG_410:g.98374C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2583C=	ENSP00000346369.2:p.Leu861=
ENST00000540630.6:c.3462C=	ENSP00000441668.3:p.Leu1154=
ENST00000613327.5:c.3408C=	ENSP00000480757.2:p.Leu1136=
ENST00000688812.1:c.*671C=	ENSP00000510658.1:n.*671C=
ENST00000690544.1:c.*2679C=	ENSP00000508989.1:n.*2679C=
ENST00000358913.10:c.3408C= MANE Select	ENSP00000351790.5:p.Leu1136=
ENST00000354393.6:c.2583C=	ENSP00000346369.2:p.Leu861=
ENST00000358913.9:c.3408C=	ENSP00000351790.5:p.Leu1136=
ENST00000540630.5:c.3408C=	ENSP00000441668.2:p.Leu1136=
ENST00000613327.4:c.2526C=	ENSP00000480757.1:p.Leu842=
NM_001256267.1:c.3408C=	NP_001243196.1:p.Leu1136=
NM_001256268.1:c.2526C=	NP_001243197.1:p.Leu842=
NM_032578.3:c.3408C= , LRG_410t1:c.3408C=	NP_115967.2:p.Leu1136=
NR_045662.3:n.2835C=
NR_045663.3:n.3537C=
XM_006718043.2:c.3462C=	XP_006718106.1:p.Leu1154=
XM_011540292.1:c.3438C=	XP_011538594.1:p.Leu1146=
XR_946029.1:n.1804-215G=
XM_017016833.1:c.3486C=	XP_016872322.1:p.Leu1162=
XM_017016834.2:c.3408C=	XP_016872323.1:p.Leu1136=
XM_024448236.1:c.2286C=	XP_024304004.1:p.Leu762=
NR_045662.4:n.2945C=
NR_045663.4:n.3482C=
NM_001256267.2:c.3408C=	NP_001243196.1:p.Leu1136=
NM_001256268.2:c.2526C=	NP_001243197.1:p.Leu842=
NM_032578.4:c.3408C= MANE Select	NP_115967.2:p.Leu1136=