Canonical Allele Identifier: CA3181375121

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199488C= , CM000672.2:g.68199488C=	GRCh38
NC_000010.10:g.69959245C= , CM000672.1:g.69959245C=	GRCh37
NC_000010.9:g.69629251C=	NCBI36
NG_032118.1:g.98372C= , LRG_410:g.98372C=

Transcript Alleles

HGVS	Amino-acid Change
NM_032578.4:c.3406C= MANE Select	NP_115967.2:p.Leu1136=
ENST00000358913.10:c.3406C= MANE Select	ENSP00000351790.5:p.Leu1136=
NM_001256267.1:c.3406C=	NP_001243196.1:p.Leu1136=
NM_001256267.2:c.3406C=	NP_001243196.1:p.Leu1136=
NM_001256268.1:c.2524C=	NP_001243197.1:p.Leu842=
NM_001256268.2:c.2524C=	NP_001243197.1:p.Leu842=
NM_032578.3:c.3406C= , LRG_410t1:c.3406C=	NP_115967.2:p.Leu1136=
NR_045662.3:n.2833C=
NR_045662.4:n.2943C=
NR_045663.3:n.3535C=
NR_045663.4:n.3480C=
ENST00000354393.6:c.2581C=	ENSP00000346369.2:p.Leu861=
ENST00000354393.7:c.2581C=	ENSP00000346369.2:p.Leu861=
ENST00000358913.9:c.3406C=	ENSP00000351790.5:p.Leu1136=
ENST00000540630.5:c.3406C=	ENSP00000441668.2:p.Leu1136=
ENST00000540630.6:c.3460C=	ENSP00000441668.3:p.Leu1154=
ENST00000613327.4:c.2524C=	ENSP00000480757.1:p.Leu842=
ENST00000613327.5:c.3406C=	ENSP00000480757.2:p.Leu1136=
ENST00000688812.1:c.*669C=	ENSP00000510658.1:n.*669C=
ENST00000690544.1:c.*2677C=	ENSP00000508989.1:n.*2677C=
XM_006718043.2:c.3460C=	XP_006718106.1:p.Leu1154=
XM_011540292.1:c.3436C=	XP_011538594.1:p.Leu1146=
XM_017016833.1:c.3484C=	XP_016872322.1:p.Leu1162=
XM_017016834.2:c.3406C=	XP_016872323.1:p.Leu1136=
XM_024448236.1:c.2284C=	XP_024304004.1:p.Leu762=
XR_946029.1:n.1804-213G=