Canonical Allele Identifier: CA1917227417

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199489T= , CM000672.2:g.68199489T=	GRCh38
NC_000010.10:g.69959246T= , CM000672.1:g.69959246T=	GRCh37
NC_000010.9:g.69629252T=	NCBI36
NG_032118.1:g.98373T= , LRG_410:g.98373T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2582T=	ENSP00000346369.2:p.Leu861=
ENST00000540630.6:c.3461T=	ENSP00000441668.3:p.Leu1154=
ENST00000613327.5:c.3407T=	ENSP00000480757.2:p.Leu1136=
ENST00000688812.1:c.*670T=	ENSP00000510658.1:n.*670T=
ENST00000690544.1:c.*2678T=	ENSP00000508989.1:n.*2678T=
ENST00000358913.10:c.3407T= MANE Select	ENSP00000351790.5:p.Leu1136=
ENST00000354393.6:c.2582T=	ENSP00000346369.2:p.Leu861=
ENST00000358913.9:c.3407T=	ENSP00000351790.5:p.Leu1136=
ENST00000540630.5:c.3407T=	ENSP00000441668.2:p.Leu1136=
ENST00000613327.4:c.2525T=	ENSP00000480757.1:p.Leu842=
NM_001256267.1:c.3407T=	NP_001243196.1:p.Leu1136=
NM_001256268.1:c.2525T=	NP_001243197.1:p.Leu842=
NM_032578.3:c.3407T= , LRG_410t1:c.3407T=	NP_115967.2:p.Leu1136=
NR_045662.3:n.2834T=
NR_045663.3:n.3536T=
XM_006718043.2:c.3461T=	XP_006718106.1:p.Leu1154=
XM_011540292.1:c.3437T=	XP_011538594.1:p.Leu1146=
XR_946029.1:n.1804-214A=
XM_017016833.1:c.3485T=	XP_016872322.1:p.Leu1162=
XM_017016834.2:c.3407T=	XP_016872323.1:p.Leu1136=
XM_024448236.1:c.2285T=	XP_024304004.1:p.Leu762=
NR_045662.4:n.2944T=
NR_045663.4:n.3481T=
NM_001256267.2:c.3407T=	NP_001243196.1:p.Leu1136=
NM_001256268.2:c.2525T=	NP_001243197.1:p.Leu842=
NM_032578.4:c.3407T= MANE Select	NP_115967.2:p.Leu1136=