Canonical Allele Identifier: CA1917227420

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199493T= , CM000672.2:g.68199493T=	GRCh38
NC_000010.10:g.69959250T= , CM000672.1:g.69959250T=	GRCh37
NC_000010.9:g.69629256T=	NCBI36
NG_032118.1:g.98377T= , LRG_410:g.98377T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2586T=	ENSP00000346369.2:p.Thr862=
ENST00000540630.6:c.3465T=	ENSP00000441668.3:p.Thr1155=
ENST00000613327.5:c.3411T=	ENSP00000480757.2:p.Thr1137=
ENST00000688812.1:c.*674T=	ENSP00000510658.1:n.*674T=
ENST00000690544.1:c.*2682T=	ENSP00000508989.1:n.*2682T=
ENST00000358913.10:c.3411T= MANE Select	ENSP00000351790.5:p.Thr1137=
ENST00000354393.6:c.2586T=	ENSP00000346369.2:p.Thr862=
ENST00000358913.9:c.3411T=	ENSP00000351790.5:p.Thr1137=
ENST00000540630.5:c.3411T=	ENSP00000441668.2:p.Thr1137=
ENST00000613327.4:c.2529T=	ENSP00000480757.1:p.Thr843=
NM_001256267.1:c.3411T=	NP_001243196.1:p.Thr1137=
NM_001256268.1:c.2529T=	NP_001243197.1:p.Thr843=
NM_032578.3:c.3411T= , LRG_410t1:c.3411T=	NP_115967.2:p.Thr1137=
NR_045662.3:n.2838T=
NR_045663.3:n.3540T=
XM_006718043.2:c.3465T=	XP_006718106.1:p.Thr1155=
XM_011540292.1:c.3441T=	XP_011538594.1:p.Thr1147=
XR_946029.1:n.1804-218A=
XM_017016833.1:c.3489T=	XP_016872322.1:p.Thr1163=
XM_017016834.2:c.3411T=	XP_016872323.1:p.Thr1137=
XM_024448236.1:c.2289T=	XP_024304004.1:p.Thr763=
NR_045662.4:n.2948T=
NR_045663.4:n.3485T=
NM_001256267.2:c.3411T=	NP_001243196.1:p.Thr1137=
NM_001256268.2:c.2529T=	NP_001243197.1:p.Thr843=
NM_032578.4:c.3411T= MANE Select	NP_115967.2:p.Thr1137=