Canonical Allele Identifier: CA376859013

Gene: MYPN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.68199414A>G , CM000672.2:g.68199414A>G	GRCh38
NC_000010.10:g.69959171A>G , CM000672.1:g.69959171A>G	GRCh37
NC_000010.9:g.69629177A>G	NCBI36
NG_032118.1:g.98298A>G , LRG_410:g.98298A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032578.4:c.3332A>G MANE Select	NP_115967.2:p.Gln1111Arg
ENST00000358913.10:c.3332A>G MANE Select	ENSP00000351790.5:p.Gln1111Arg
NM_001256267.1:c.3332A>G	NP_001243196.1:p.Gln1111Arg
NM_001256267.2:c.3332A>G	NP_001243196.1:p.Gln1111Arg
NM_001256268.1:c.2450A>G	NP_001243197.1:p.Gln817Arg
NM_001256268.2:c.2450A>G	NP_001243197.1:p.Gln817Arg
NM_032578.3:c.3332A>G , LRG_410t1:c.3332A>G	NP_115967.2:p.Gln1111Arg
NR_045662.3:n.2759A>G
NR_045662.4:n.2869A>G
NR_045663.3:n.3461A>G
NR_045663.4:n.3406A>G
ENST00000354393.6:c.2507A>G	ENSP00000346369.2:p.Gln836Arg
ENST00000354393.7:c.2507A>G	ENSP00000346369.2:p.Gln836Arg
ENST00000358913.9:c.3332A>G	ENSP00000351790.5:p.Gln1111Arg
ENST00000540630.5:c.3332A>G	ENSP00000441668.2:p.Gln1111Arg
ENST00000540630.6:c.3386A>G	ENSP00000441668.3:p.Gln1129Arg
ENST00000613327.4:c.2450A>G	ENSP00000480757.1:p.Gln817Arg
ENST00000613327.5:c.3332A>G	ENSP00000480757.2:p.Gln1111Arg
ENST00000688812.1:c.*595A>G	ENSP00000510658.1:n.*595A>G
ENST00000690544.1:c.*2603A>G	ENSP00000508989.1:n.*2603A>G
XM_006718043.2:c.3386A>G	XP_006718106.1:p.Gln1129Arg
XM_011540292.1:c.3362A>G	XP_011538594.1:p.Gln1121Arg
XM_017016833.1:c.3410A>G	XP_016872322.1:p.Gln1137Arg
XM_017016834.2:c.3332A>G	XP_016872323.1:p.Gln1111Arg
XM_024448236.1:c.2210A>G	XP_024304004.1:p.Gln737Arg
XR_946029.1:n.1804-139T>C