Canonical Allele Identifier: CA3181375111

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199483A= , CM000672.2:g.68199483A=	GRCh38
NC_000010.10:g.69959240A= , CM000672.1:g.69959240A=	GRCh37
NC_000010.9:g.69629246A=	NCBI36
NG_032118.1:g.98367A= , LRG_410:g.98367A=

Transcript Alleles

HGVS	Amino-acid Change
NM_032578.4:c.3401A= MANE Select	NP_115967.2:p.Asp1134=
ENST00000358913.10:c.3401A= MANE Select	ENSP00000351790.5:p.Asp1134=
NM_001256267.1:c.3401A=	NP_001243196.1:p.Asp1134=
NM_001256267.2:c.3401A=	NP_001243196.1:p.Asp1134=
NM_001256268.1:c.2519A=	NP_001243197.1:p.Asp840=
NM_001256268.2:c.2519A=	NP_001243197.1:p.Asp840=
NM_032578.3:c.3401A= , LRG_410t1:c.3401A=	NP_115967.2:p.Asp1134=
NR_045662.3:n.2828A=
NR_045662.4:n.2938A=
NR_045663.3:n.3530A=
NR_045663.4:n.3475A=
ENST00000354393.6:c.2576A=	ENSP00000346369.2:p.Asp859=
ENST00000354393.7:c.2576A=	ENSP00000346369.2:p.Asp859=
ENST00000358913.9:c.3401A=	ENSP00000351790.5:p.Asp1134=
ENST00000540630.5:c.3401A=	ENSP00000441668.2:p.Asp1134=
ENST00000540630.6:c.3455A=	ENSP00000441668.3:p.Asp1152=
ENST00000613327.4:c.2519A=	ENSP00000480757.1:p.Asp840=
ENST00000613327.5:c.3401A=	ENSP00000480757.2:p.Asp1134=
ENST00000688812.1:c.*664A=	ENSP00000510658.1:n.*664A=
ENST00000690544.1:c.*2672A=	ENSP00000508989.1:n.*2672A=
XM_006718043.2:c.3455A=	XP_006718106.1:p.Asp1152=
XM_011540292.1:c.3431A=	XP_011538594.1:p.Asp1144=
XM_017016833.1:c.3479A=	XP_016872322.1:p.Asp1160=
XM_017016834.2:c.3401A=	XP_016872323.1:p.Asp1134=
XM_024448236.1:c.2279A=	XP_024304004.1:p.Asp760=
XR_946029.1:n.1804-208T=