Canonical Allele Identifier: CA1917227381

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199401C= , CM000672.2:g.68199401C=	GRCh38
NC_000010.10:g.69959158C= , CM000672.1:g.69959158C=	GRCh37
NC_000010.9:g.69629164C=	NCBI36
NG_032118.1:g.98285C= , LRG_410:g.98285C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2494C=	ENSP00000346369.2:p.Leu832=
ENST00000540630.6:c.3373C=	ENSP00000441668.3:p.Leu1125=
ENST00000613327.5:c.3319C=	ENSP00000480757.2:p.Leu1107=
ENST00000688812.1:c.*582C=	ENSP00000510658.1:n.*582C=
ENST00000690544.1:c.*2590C=	ENSP00000508989.1:n.*2590C=
ENST00000358913.10:c.3319C= MANE Select	ENSP00000351790.5:p.Leu1107=
ENST00000354393.6:c.2494C=	ENSP00000346369.2:p.Leu832=
ENST00000358913.9:c.3319C=	ENSP00000351790.5:p.Leu1107=
ENST00000540630.5:c.3319C=	ENSP00000441668.2:p.Leu1107=
ENST00000613327.4:c.2437C=	ENSP00000480757.1:p.Leu813=
NM_001256267.1:c.3319C=	NP_001243196.1:p.Leu1107=
NM_001256268.1:c.2437C=	NP_001243197.1:p.Leu813=
NM_032578.3:c.3319C= , LRG_410t1:c.3319C=	NP_115967.2:p.Leu1107=
NR_045662.3:n.2746C=
NR_045663.3:n.3448C=
XM_006718043.2:c.3373C=	XP_006718106.1:p.Leu1125=
XM_011540292.1:c.3349C=	XP_011538594.1:p.Leu1117=
XR_946029.1:n.1804-126G=
XM_017016833.1:c.3397C=	XP_016872322.1:p.Leu1133=
XM_017016834.2:c.3319C=	XP_016872323.1:p.Leu1107=
XM_024448236.1:c.2197C=	XP_024304004.1:p.Leu733=
NR_045662.4:n.2856C=
NR_045663.4:n.3393C=
NM_001256267.2:c.3319C=	NP_001243196.1:p.Leu1107=
NM_001256268.2:c.2437C=	NP_001243197.1:p.Leu813=
NM_032578.4:c.3319C= MANE Select	NP_115967.2:p.Leu1107=