Canonical Allele Identifier: CA1917232445

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68210431T= , CM000672.2:g.68210431T=	GRCh38
NC_000010.10:g.69970188T= , CM000672.1:g.69970188T=	GRCh37
NC_000010.9:g.69640194T=	NCBI36
NG_032118.1:g.109315T= , LRG_410:g.109315T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.3114T=	ENSP00000346369.2:p.Ser1038=
ENST00000540630.6:c.3993T=	ENSP00000441668.3:p.Ser1331=
ENST00000613327.5:c.3939T=	ENSP00000480757.2:p.Ser1313=
ENST00000688812.1:c.*1202T=	ENSP00000510658.1:n.*1202T=
ENST00000690544.1:c.*3210T=	ENSP00000508989.1:n.*3210T=
ENST00000358913.10:c.3939T= MANE Select	ENSP00000351790.5:p.Ser1313=
ENST00000354393.6:c.3114T=	ENSP00000346369.2:p.Ser1038=
ENST00000358913.9:c.3939T=	ENSP00000351790.5:p.Ser1313=
ENST00000540630.5:c.3939T=	ENSP00000441668.2:p.Ser1313=
ENST00000613327.4:c.3057T=	ENSP00000480757.1:p.Ser1019=
NM_001256267.1:c.3939T=	NP_001243196.1:p.Ser1313=
NM_001256268.1:c.3057T=	NP_001243197.1:p.Ser1019=
NM_032578.3:c.3939T= , LRG_410t1:c.3939T=	NP_115967.2:p.Ser1313=
NR_045662.3:n.3366T=
NR_045663.3:n.4068T=
XM_006718043.2:c.3993T=	XP_006718106.1:p.Ser1331=
XM_011540292.1:c.3969T=	XP_011538594.1:p.Ser1323=
XR_946029.1:n.1574+4857A=
XM_017016833.1:c.4017T=	XP_016872322.1:p.Ser1339=
XM_017016834.2:c.3939T=	XP_016872323.1:p.Ser1313=
XM_024448236.1:c.2817T=	XP_024304004.1:p.Ser939=
NR_045662.4:n.3476T=
NR_045663.4:n.4013T=
NM_001256267.2:c.3939T=	NP_001243196.1:p.Ser1313=
NM_001256268.2:c.3057T=	NP_001243197.1:p.Ser1019=
NM_032578.4:c.3939T= MANE Select	NP_115967.2:p.Ser1313=