Canonical Allele Identifier: CA1630848291

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68166562C= , CM000672.2:g.68166562C=	GRCh38
NC_000010.10:g.69926319C= , CM000672.1:g.69926319C=	GRCh37
NC_000010.9:g.69596325C=	NCBI36
NG_032118.1:g.65446C= , LRG_410:g.65446C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.1044C=	ENSP00000346369.2:p.Thr348=
ENST00000373675.4:c.1869C=	ENSP00000362779.4:p.Thr623=
ENST00000540630.6:c.1923C=	ENSP00000441668.3:p.Thr641=
ENST00000613327.5:c.1869C=	ENSP00000480757.2:p.Thr623=
ENST00000687572.1:c.747C=	ENSP00000510427.1:p.Thr249=
ENST00000688812.1:c.1845C=	ENSP00000510658.1:p.Thr615=
ENST00000690544.1:c.*1140C=	ENSP00000508989.1:n.*1140C=
ENST00000358913.10:c.1869C= MANE Select	ENSP00000351790.5:p.Thr623=
ENST00000354393.6:c.1044C=	ENSP00000346369.2:p.Thr348=
ENST00000358913.9:c.1869C=	ENSP00000351790.5:p.Thr623=
ENST00000540630.5:c.1869C=	ENSP00000441668.2:p.Thr623=
ENST00000613327.4:c.987C=	ENSP00000480757.1:p.Thr329=
NM_001256267.1:c.1869C=	NP_001243196.1:p.Thr623=
NM_001256268.1:c.987C=	NP_001243197.1:p.Thr329=
NM_032578.3:c.1869C= , LRG_410t1:c.1869C=	NP_115967.2:p.Thr623=
NR_045662.3:n.1296C=
NR_045663.3:n.2137C=
XM_006718043.2:c.1923C=	XP_006718106.1:p.Thr641=
XM_011540292.1:c.1899C=	XP_011538594.1:p.Thr633=
XM_017016833.1:c.1947C=	XP_016872322.1:p.Thr649=
XM_017016834.2:c.1869C=	XP_016872323.1:p.Thr623=
XM_024448236.1:c.747C=	XP_024304004.1:p.Thr249=
NR_045662.4:n.1406C=
NR_045663.4:n.2082C=
NM_001256267.2:c.1869C=	NP_001243196.1:p.Thr623=
NM_001256268.2:c.987C=	NP_001243197.1:p.Thr329=
NM_032578.4:c.1869C= MANE Select	NP_115967.2:p.Thr623=