Canonical Allele Identifier: CA1917232399

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68210325G= , CM000672.2:g.68210325G=	GRCh38
NC_000010.10:g.69970082G= , CM000672.1:g.69970082G=	GRCh37
NC_000010.9:g.69640088G=	NCBI36
NG_032118.1:g.109209G= , LRG_410:g.109209G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.3008G=	ENSP00000346369.2:p.Arg1003=
ENST00000540630.6:c.3887G=	ENSP00000441668.3:p.Arg1296=
ENST00000613327.5:c.3833G=	ENSP00000480757.2:p.Arg1278=
ENST00000688812.1:c.*1096G=	ENSP00000510658.1:n.*1096G=
ENST00000690544.1:c.*3104G=	ENSP00000508989.1:n.*3104G=
ENST00000358913.10:c.3833G= MANE Select	ENSP00000351790.5:p.Arg1278=
ENST00000354393.6:c.3008G=	ENSP00000346369.2:p.Arg1003=
ENST00000358913.9:c.3833G=	ENSP00000351790.5:p.Arg1278=
ENST00000540630.5:c.3833G=	ENSP00000441668.2:p.Arg1278=
ENST00000613327.4:c.2951G=	ENSP00000480757.1:p.Arg984=
NM_001256267.1:c.3833G=	NP_001243196.1:p.Arg1278=
NM_001256268.1:c.2951G=	NP_001243197.1:p.Arg984=
NM_032578.3:c.3833G= , LRG_410t1:c.3833G=	NP_115967.2:p.Arg1278=
NR_045662.3:n.3260G=
NR_045663.3:n.3962G=
XM_006718043.2:c.3887G=	XP_006718106.1:p.Arg1296=
XM_011540292.1:c.3863G=	XP_011538594.1:p.Arg1288=
XR_946029.1:n.1574+4963C=
XM_017016833.1:c.3911G=	XP_016872322.1:p.Arg1304=
XM_017016834.2:c.3833G=	XP_016872323.1:p.Arg1278=
XM_024448236.1:c.2711G=	XP_024304004.1:p.Arg904=
NR_045662.4:n.3370G=
NR_045663.4:n.3907G=
NM_001256267.2:c.3833G=	NP_001243196.1:p.Arg1278=
NM_001256268.2:c.2951G=	NP_001243197.1:p.Arg984=
NM_032578.4:c.3833G= MANE Select	NP_115967.2:p.Arg1278=