Canonical Allele Identifier: CA1917230846

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68206903G= , CM000672.2:g.68206903G=	GRCh38
NC_000010.10:g.69966660G= , CM000672.1:g.69966660G=	GRCh37
NC_000010.9:g.69636666G=	NCBI36
NG_032118.1:g.105787G= , LRG_410:g.105787G=

Transcript Alleles

HGVS	Amino-acid Change
NM_032578.4:c.3793G= MANE Select	NP_115967.2:p.Ala1265=
ENST00000358913.10:c.3793G= MANE Select	ENSP00000351790.5:p.Ala1265=
NM_001256267.1:c.3793G=	NP_001243196.1:p.Ala1265=
NM_001256267.2:c.3793G=	NP_001243196.1:p.Ala1265=
NM_001256268.1:c.2911G=	NP_001243197.1:p.Ala971=
NM_001256268.2:c.2911G=	NP_001243197.1:p.Ala971=
NM_032578.3:c.3793G= , LRG_410t1:c.3793G=	NP_115967.2:p.Ala1265=
NR_045662.3:n.3220G=
NR_045662.4:n.3330G=
NR_045663.3:n.3922G=
NR_045663.4:n.3867G=
ENST00000354393.6:c.2968G=	ENSP00000346369.2:p.Ala990=
ENST00000354393.7:c.2968G=	ENSP00000346369.2:p.Ala990=
ENST00000358913.9:c.3793G=	ENSP00000351790.5:p.Ala1265=
ENST00000540630.5:c.3793G=	ENSP00000441668.2:p.Ala1265=
ENST00000540630.6:c.3847G=	ENSP00000441668.3:p.Ala1283=
ENST00000613327.4:c.2911G=	ENSP00000480757.1:p.Ala971=
ENST00000613327.5:c.3793G=	ENSP00000480757.2:p.Ala1265=
ENST00000688812.1:c.*1056G=	ENSP00000510658.1:n.*1056G=
ENST00000690544.1:c.*3064G=	ENSP00000508989.1:n.*3064G=
XM_006718043.2:c.3847G=	XP_006718106.1:p.Ala1283=
XM_011540292.1:c.3823G=	XP_011538594.1:p.Ala1275=
XM_017016833.1:c.3871G=	XP_016872322.1:p.Ala1291=
XM_017016834.2:c.3793G=	XP_016872323.1:p.Ala1265=
XM_024448236.1:c.2671G=	XP_024304004.1:p.Ala891=
XR_946029.1:n.1575-2644C=