Canonical Allele Identifier: CA1917227379

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199396C= , CM000672.2:g.68199396C=	GRCh38
NC_000010.10:g.69959153C= , CM000672.1:g.69959153C=	GRCh37
NC_000010.9:g.69629159C=	NCBI36
NG_032118.1:g.98280C= , LRG_410:g.98280C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2489C=	ENSP00000346369.2:p.Thr830=
ENST00000540630.6:c.3368C=	ENSP00000441668.3:p.Thr1123=
ENST00000613327.5:c.3314C=	ENSP00000480757.2:p.Thr1105=
ENST00000688812.1:c.*577C=	ENSP00000510658.1:n.*577C=
ENST00000690544.1:c.*2585C=	ENSP00000508989.1:n.*2585C=
ENST00000358913.10:c.3314C= MANE Select	ENSP00000351790.5:p.Thr1105=
ENST00000354393.6:c.2489C=	ENSP00000346369.2:p.Thr830=
ENST00000358913.9:c.3314C=	ENSP00000351790.5:p.Thr1105=
ENST00000540630.5:c.3314C=	ENSP00000441668.2:p.Thr1105=
ENST00000613327.4:c.2432C=	ENSP00000480757.1:p.Thr811=
NM_001256267.1:c.3314C=	NP_001243196.1:p.Thr1105=
NM_001256268.1:c.2432C=	NP_001243197.1:p.Thr811=
NM_032578.3:c.3314C= , LRG_410t1:c.3314C=	NP_115967.2:p.Thr1105=
NR_045662.3:n.2741C=
NR_045663.3:n.3443C=
XM_006718043.2:c.3368C=	XP_006718106.1:p.Thr1123=
XM_011540292.1:c.3344C=	XP_011538594.1:p.Thr1115=
XR_946029.1:n.1804-121G=
XM_017016833.1:c.3392C=	XP_016872322.1:p.Thr1131=
XM_017016834.2:c.3314C=	XP_016872323.1:p.Thr1105=
XM_024448236.1:c.2192C=	XP_024304004.1:p.Thr731=
NR_045662.4:n.2851C=
NR_045663.4:n.3388C=
NM_001256267.2:c.3314C=	NP_001243196.1:p.Thr1105=
NM_001256268.2:c.2432C=	NP_001243197.1:p.Thr811=
NM_032578.4:c.3314C= MANE Select	NP_115967.2:p.Thr1105=