Canonical Allele Identifier: CA1917227383

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199404C= , CM000672.2:g.68199404C=	GRCh38
NC_000010.10:g.69959161C= , CM000672.1:g.69959161C=	GRCh37
NC_000010.9:g.69629167C=	NCBI36
NG_032118.1:g.98288C= , LRG_410:g.98288C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2497C=	ENSP00000346369.2:p.Leu833=
ENST00000540630.6:c.3376C=	ENSP00000441668.3:p.Leu1126=
ENST00000613327.5:c.3322C=	ENSP00000480757.2:p.Leu1108=
ENST00000688812.1:c.*585C=	ENSP00000510658.1:n.*585C=
ENST00000690544.1:c.*2593C=	ENSP00000508989.1:n.*2593C=
ENST00000358913.10:c.3322C= MANE Select	ENSP00000351790.5:p.Leu1108=
ENST00000354393.6:c.2497C=	ENSP00000346369.2:p.Leu833=
ENST00000358913.9:c.3322C=	ENSP00000351790.5:p.Leu1108=
ENST00000540630.5:c.3322C=	ENSP00000441668.2:p.Leu1108=
ENST00000613327.4:c.2440C=	ENSP00000480757.1:p.Leu814=
NM_001256267.1:c.3322C=	NP_001243196.1:p.Leu1108=
NM_001256268.1:c.2440C=	NP_001243197.1:p.Leu814=
NM_032578.3:c.3322C= , LRG_410t1:c.3322C=	NP_115967.2:p.Leu1108=
NR_045662.3:n.2749C=
NR_045663.3:n.3451C=
XM_006718043.2:c.3376C=	XP_006718106.1:p.Leu1126=
XM_011540292.1:c.3352C=	XP_011538594.1:p.Leu1118=
XR_946029.1:n.1804-129G=
XM_017016833.1:c.3400C=	XP_016872322.1:p.Leu1134=
XM_017016834.2:c.3322C=	XP_016872323.1:p.Leu1108=
XM_024448236.1:c.2200C=	XP_024304004.1:p.Leu734=
NR_045662.4:n.2859C=
NR_045663.4:n.3396C=
NM_001256267.2:c.3322C=	NP_001243196.1:p.Leu1108=
NM_001256268.2:c.2440C=	NP_001243197.1:p.Leu814=
NM_032578.4:c.3322C= MANE Select	NP_115967.2:p.Leu1108=