Canonical Allele Identifier: CA1917227373

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199384C= , CM000672.2:g.68199384C=	GRCh38
NC_000010.10:g.69959141C= , CM000672.1:g.69959141C=	GRCh37
NC_000010.9:g.69629147C=	NCBI36
NG_032118.1:g.98268C= , LRG_410:g.98268C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.2477C=	ENSP00000346369.2:p.Pro826=
ENST00000540630.6:c.3356C=	ENSP00000441668.3:p.Pro1119=
ENST00000613327.5:c.3302C=	ENSP00000480757.2:p.Pro1101=
ENST00000688812.1:c.*565C=	ENSP00000510658.1:n.*565C=
ENST00000690544.1:c.*2573C=	ENSP00000508989.1:n.*2573C=
ENST00000358913.10:c.3302C= MANE Select	ENSP00000351790.5:p.Pro1101=
ENST00000354393.6:c.2477C=	ENSP00000346369.2:p.Pro826=
ENST00000358913.9:c.3302C=	ENSP00000351790.5:p.Pro1101=
ENST00000540630.5:c.3302C=	ENSP00000441668.2:p.Pro1101=
ENST00000613327.4:c.2420C=	ENSP00000480757.1:p.Pro807=
NM_001256267.1:c.3302C=	NP_001243196.1:p.Pro1101=
NM_001256268.1:c.2420C=	NP_001243197.1:p.Pro807=
NM_032578.3:c.3302C= , LRG_410t1:c.3302C=	NP_115967.2:p.Pro1101=
NR_045662.3:n.2729C=
NR_045663.3:n.3431C=
XM_006718043.2:c.3356C=	XP_006718106.1:p.Pro1119=
XM_011540292.1:c.3332C=	XP_011538594.1:p.Pro1111=
XR_946029.1:n.1804-109G=
XM_017016833.1:c.3380C=	XP_016872322.1:p.Pro1127=
XM_017016834.2:c.3302C=	XP_016872323.1:p.Pro1101=
XM_024448236.1:c.2180C=	XP_024304004.1:p.Pro727=
NR_045662.4:n.2839C=
NR_045663.4:n.3376C=
NM_001256267.2:c.3302C=	NP_001243196.1:p.Pro1101=
NM_001256268.2:c.2420C=	NP_001243197.1:p.Pro807=
NM_032578.4:c.3302C= MANE Select	NP_115967.2:p.Pro1101=