Canonical Allele Identifier: CA1917227367

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199375G= , CM000672.2:g.68199375G=	GRCh38
NC_000010.10:g.69959132G= , CM000672.1:g.69959132G=	GRCh37
NC_000010.9:g.69629138G=	NCBI36
NG_032118.1:g.98259G= , LRG_410:g.98259G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2468G=	ENSP00000346369.2:p.Gly823=
ENST00000540630.6:c.3347G=	ENSP00000441668.3:p.Gly1116=
ENST00000613327.5:c.3293G=	ENSP00000480757.2:p.Gly1098=
ENST00000688812.1:c.*556G=	ENSP00000510658.1:n.*556G=
ENST00000690544.1:c.*2564G=	ENSP00000508989.1:n.*2564G=
ENST00000358913.10:c.3293G= MANE Select	ENSP00000351790.5:p.Gly1098=
ENST00000354393.6:c.2468G=	ENSP00000346369.2:p.Gly823=
ENST00000358913.9:c.3293G=	ENSP00000351790.5:p.Gly1098=
ENST00000540630.5:c.3293G=	ENSP00000441668.2:p.Gly1098=
ENST00000613327.4:c.2411G=	ENSP00000480757.1:p.Gly804=
NM_001256267.1:c.3293G=	NP_001243196.1:p.Gly1098=
NM_001256268.1:c.2411G=	NP_001243197.1:p.Gly804=
NM_032578.3:c.3293G= , LRG_410t1:c.3293G=	NP_115967.2:p.Gly1098=
NR_045662.3:n.2720G=
NR_045663.3:n.3422G=
XM_006718043.2:c.3347G=	XP_006718106.1:p.Gly1116=
XM_011540292.1:c.3323G=	XP_011538594.1:p.Gly1108=
XR_946029.1:n.1804-100C=
XM_017016833.1:c.3371G=	XP_016872322.1:p.Gly1124=
XM_017016834.2:c.3293G=	XP_016872323.1:p.Gly1098=
XM_024448236.1:c.2171G=	XP_024304004.1:p.Gly724=
NR_045662.4:n.2830G=
NR_045663.4:n.3367G=
NM_001256267.2:c.3293G=	NP_001243196.1:p.Gly1098=
NM_001256268.2:c.2411G=	NP_001243197.1:p.Gly804=
NM_032578.4:c.3293G= MANE Select	NP_115967.2:p.Gly1098=