Canonical Allele Identifier: CA1917232566

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68210693C= , CM000672.2:g.68210693C=	GRCh38
NC_000010.10:g.69970450C= , CM000672.1:g.69970450C=	GRCh37
NC_000010.9:g.69640456C=	NCBI36
NG_032118.1:g.109577C= , LRG_410:g.109577C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354393.7:c.*238C=	ENSP00000346369.2:n.*238C=
ENST00000540630.6:c.*238C=	ENSP00000441668.3:n.*238C=
ENST00000613327.5:c.*238C=	ENSP00000480757.2:n.*238C=
ENST00000688812.1:c.*1464C=	ENSP00000510658.1:n.*1464C=
ENST00000690544.1:c.*3472C=	ENSP00000508989.1:n.*3472C=
ENST00000358913.10:c.*238C= MANE Select	ENSP00000351790.5:n.*238C=
ENST00000354393.6:c.*238C=	ENSP00000346369.2:n.*238C=
ENST00000358913.9:c.*238C=	ENSP00000351790.5:n.*238C=
ENST00000540630.5:c.*238C=	ENSP00000441668.2:n.*238C=
ENST00000613327.4:c.*238C=	ENSP00000480757.1:n.*238C=
NM_001256267.1:c.*238C=	NP_001243196.1:n.*238C=
NM_001256268.1:c.*238C=	NP_001243197.1:n.*238C=
NM_032578.3:c.*238C= , LRG_410t1:c.*238C=	NP_115967.2:n.*238C=
NR_045662.3:n.3628C=
NR_045663.3:n.4330C=
XM_006718043.2:c.*238C=	XP_006718106.1:n.*238C=
XM_011540292.1:c.*238C=	XP_011538594.1:n.*238C=
XR_946029.1:n.1574+4595G=
XM_017016833.1:c.*238C=	XP_016872322.1:n.*238C=
XM_017016834.2:c.*238C=	XP_016872323.1:n.*238C=
XM_024448236.1:c.*238C=	XP_024304004.1:n.*238C=
NR_045662.4:n.3738C=
NR_045663.4:n.4275C=
NM_001256267.2:c.*238C=	NP_001243196.1:n.*238C=
NM_001256268.2:c.*238C=	NP_001243197.1:n.*238C=
NM_032578.4:c.*238C= MANE Select	NP_115967.2:n.*238C=